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

RNF19A

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs186652209	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257654	GTTTATCTATTTCCT[A/G]TATTTTTATATATAA	25897
rs186658058	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100279824	GAGCCACCACACCCA[A/G]CCTCAATTTTTTGTG	25897
rs186661408	snp	C/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100328705	TCAAACTCCTGACCT[C/G]GTGATTCACCCCCAT	25897
rs186664481	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288486	TAAAAGATTCTAGAT[A/T]TGAGCTGACCAGAAA	25897
rs186667482	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100307853	TGAATGAAGTATCTT[C/T]AAAAATAGGAATCTT	25897
rs186734280	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100331266	TGAACCTTGATTTCA[C/T]ATAATGTAGAAAAGC	25897
rs186751960	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100290603	GTCCCTCGGTTTATA[C/T]TTCCCTTCACAAACA	25897
rs186778940	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100326698	AGCTCTTGAATTCAT[A/T]CCCTTCTTCCCTCTT	25897
rs186791929	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287164	TAACCCCCTCATCAT[A/G]AACAAACCTGATCAT	25897
rs186799573	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100262496	GGATAATGCTTGGCA[C/T]CCTCAAAAATCAAGC	25897
rs186804523	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284736	CCAAAATATCCCAAA[A/G]TATGAGTTTCTGATT	25897
rs186977372	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100306763	TTAGCTGTGCAGGTA[C/T]GGTTAAGTAAATGAG	25897
rs186996612	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100267235	CTGCTTCTTTGTGTG[C/T]AACTGAAGATATATT	25897
rs187005478	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318324	GTATAAGATTTAAAA[C/G]GATGTATTTTATATA	25897
rs187013453	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100338189	TCTCCATGTTGGCCA[G/T]GCTGGTCTCGAACTC	25897
rs187226080	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100333503	GATTGCTTATACAGC[A/G]AGATCAGTACCATAT	25897
rs187232887	snp	C/T	0.0154538	0.0865337	intron-variant	RNF19A	GRCh38.p7	8:100314799	TATAATTTTTCTGTA[C/T]AAAGTACTTCATTGT	25897
rs187261842	snp	C/T	0.00478085	0.0486577	intron-variant	RNF19A	GRCh38.p7	8:100293363	ACGTTTTATGGATAT[C/T]TTTGCTGAATACAGA	25897
rs187265015	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100274621	AACTCCTGGCCTTAA[G/T]TGGTCGGCCCGCCTC	25897
rs187280299	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100323595	AGTTTTTAAAATTTC[A/G]TCTACCTTTGCCAGG	25897
rs187283334	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100285092	TTTTGTTGTTGTTAT[C/G/T]GTGGAACATCCCTGT	25897
rs187288577	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304816	TTTACACTGAGCCTT[A/G]CTCTGACTAGTTACT	25897
rs187293998	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100263900	CAGTTTATTCACTTA[C/T]GTACTTCTGAATGAA	25897
rs187364870	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278183	AAAATAATCTTTGGC[C/T]TTGGCCTTGGCCTTT	25897
rs187385723	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100277143	CTTTTGTAAATACTA[A/G]ACATTTCCTTTTGCC	25897
rs187393091	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100297828	AAATATAATAAGATG[A/C]GGTAACAAAATTTAG	25897
rs187393974	snp	A/G	0.0023933	0.0345097	downstream-variant-500B	RNF19A	GRCh38.p7	8:100256604	GAAGCTACAAGAATA[A/G]AAAGCATCTGATTAC	25897
rs187455845	snp	C/T	0.00517822	0.0506191	intron-variant	RNF19A	GRCh38.p7	8:100299597	AAACACTGTCTCTAC[C/T]AGAAATACAAAATTA	25897
rs187507834	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100268451	AACTTTCATTAAAAA[G/T]ATCTCATAGACCTGA	25897
rs187616033	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100327396	AGCTGGAATTACAGG[A/C/T]GTGTGCCACCATGCC	25897
rs187630318	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100296085	ATGCATTCTCTGGGC[A/G]TTATTCTTTTTTTTC	25897
rs187719968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315463	CCATCATTTCACCTG[A/G]CTTAGGGAGGCAGTC	25897
rs187727686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320116	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT	25897
rs187737509	snp	C/T	0.00358779	0.0422022	intron-variant	RNF19A	GRCh38.p7	8:100334185	CCTTTGCCAAACTCT[C/T]GGAGCATGTTCTTTT	25897
rs187938715	snp	A/G	0.00318978	0.0398085	intron-variant	RNF19A	GRCh38.p7	8:100328891	CCAGGTGAGCAGGTC[A/G]TAAGGGAATAGGACC	25897
rs187975409	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330407	GTCATGACCTGTAAG[G/T]GTTATGATCTTTGCC	25897
rs187978746	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288792	TAGGCCAGGCGCGGT[G/T]GCTCACGCCTGTAAT	25897
rs188047423	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100267943	TCAGCCTTCCAAAGT[C/G]CTAAGATTACAGGGG	25897
rs188116763	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100313642	TAGATGTTTAAGCAG[C/T]GTGACATCTGATTTG	25897
rs188122666	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274453	AACATTTATGTTACA[A/G]AAGTATTAAATGTCG	25897
rs188233766	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302996	AATTAGAATTCTAAC[A/G]AAAGAGCTGTTTAGT	25897
rs188252296	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100269202	ACTGATAACTGAAAT[C/T]CAGGTTAAAAATTTA	25897
rs188254186	snp	C/T	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100308506	TTAAAGAAGCAAAAA[C/T]AGGCAAACAGGGTAA	25897
rs188273958	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100261966	TTTTCAAAAACCCAG[A/G]TTTAGGAATTCTATA	25897
rs188365768	snp	G/T	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100332966	ATGGGTTCTCTTTTT[G/T]CTTTGTCTTATTTAC	25897
rs188411207	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292838	CCATTGCTCTATAAG[C/T]TTACCAAGTCTTCTT	25897
rs188515636	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100322844	AGTGGAGTAGTCAGA[A/G]CACACACACACATTT	25897
rs188544993	snp	G/T	0.00438332	0.0466095	intron-variant	RNF19A	GRCh38.p7	8:100284185	AGTAATAGCATTAAA[G/T]ATCTCACTTAATCCT	25897
rs188595664	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325926	AAACATATCAGACAC[A/C]GTCCATGTCTGAACA	25897
rs188605405	snp	G/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100306328	ACAACTGAACACTTC[G/T]GTCATATTGAGAGTT	25897
rs188626001	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287130	AATAAAGAAGGTCAT[G/T]TGAATTTATGACCAC	25897
rs188629875	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100299898	TTGGAAGCTCATTTG[C/T]CTCTTTCTCCTAAAG	25897
rs188642498	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100281006	AAAGAACAGGCTCAA[C/T]AGAAGGTCATGGAAA	25897
rs188644714	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320938	GTGTAAAAATGTATA[C/T]ACCTTAATTTAAAAA	25897
rs188655461	snp	A/C/T	0.00103695	0.0227477	intron-variant	RNF19A	GRCh38.p7	8:100259804	TAATGATAGGAATTA[A/C/T]TCCTTTAATTTAAAA	25897
rs188768755	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100323249	TGAAGGTAGTATTTC[A/C]TAGAAAGTTTTTAAG	25897
rs188877371	snp	G/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100319003	ATAATGCTGTGAGAG[G/T]TTGTAGGGACTGGCA	25897
rs188878113	snp	C/T	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100295083	GAACTTTCATTCCAG[C/T]ACATTTAAGCATTGA	25897
rs188893271	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100315993	CACTGACTTCAAGAA[C/T]GAAGCCGTGGACCCT	25897
rs188906467	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279337	AATCCTGCATTACCA[C/T]GTCAAACATTTAATA	25897
rs188909784	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100276876	CAGAAATAACTAGAA[A/G]TAAATCAGGAAATTT	25897
rs188999775	snp	A/G	0.0115144	0.0749975	intron-variant	RNF19A	GRCh38.p7	8:100270919	CTACTTTGCATGTTG[A/G]CATCTGTTTAAATAG	25897
rs189033606	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303878	GGAGGCGGAGGGTGC[A/G]GTAAGCCAAGATTGC	25897
rs189167646	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100298339	CTCAAAGGTAAATTA[C/T]ATAAATAATGTACAG	25897
rs189201117	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF19A	GRCh38.p7	8:100257002	TATGAATACTACCAC[A/G]TGGCCAATGAATATT	25897
rs189253427	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336311	CGTCCTGCTGGCCAA[A/C]CACAATGAGTCTGCA	25897
rs189276914	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100286460	TTTGAATGTTGTATA[C/T]TACATAGAAATCCTT	25897
rs189289602	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100305646	AATAAATACCTTAGA[C/T]TGTAGATACTTTAAT	25897
rs189291374	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100266315	ACATGTTTGAAAAAA[A/G]GAGATCTGTAACTGT	25897
rs189299882	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100290491	AAACTCATGATTAAT[A/G]TGCCTTTTTCTATGT	25897
rs189403349	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100328985	GGAATCTGGGTCTTG[C/T]GCAGGTTTATCAGTT	25897
rs189409348	snp	A/G	0.0111196	0.0737302	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100310078	TCGACGGCTGCTCCC[A/G]GGAACCAGCGCCGCA	25897
rs189441461	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100270092	TTTACCAATTGTAGC[A/G]CTGTCAAAAAATCTT	25897
rs189442994	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289220	TGGATGGATGGCTCA[C/T]CCATGTGTGAAAATC	25897
rs189506236	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100290907	GATGTTTCATTTCTT[C/T]GGCTCTCCGATATCC	25897
rs189516955	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100331506	GCTGGGCATGGTGGC[A/G]TGCACCAGCAGTCCC	25897
rs189533842	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100261028	CAACGATTTATAATA[G/T]AAAATGTGACAAGGA	25897
rs189537592	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100300780	AGTCAACTCCTGGGA[A/G]ACAGTAATCCAAAGA	25897
rs189543489	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100283109	CAGAGACAATAAATC[A/G]TTAATTATGTCCCAG	25897
rs189658903	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315754	ACTCAAGCGATCCTC[C/T]CACCTCAGCCTCCTG	25897
rs189694832	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276051	TTCTCCGAGTTAATA[C/T]TTCTGACACTTTAAA	25897
rs189773327	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311223	AAGCTAGGCAGTTTA[A/G]GTTTAAGTGTCTTTG	25897
rs189802042	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271721	CTTTCACTCTCTGTA[C/T]ACTTATTTATCTATG	25897
rs189830969	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100264562	CCAAGACTTACTGCA[A/G]GCTCAATTTAAATTG	25897
rs189835364	snp	A/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305339	GTGTATGCAATTCTG[A/T]ATTTGGCCTCAAAAG	25897
rs189928785	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100294106	TGAGGGAGTCTTGAC[A/G]TGGAATGAAGCATAT	25897
rs189932851	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334931	AGGCACCAAGATAAG[A/C]TAATGGGTAGATAGA	25897
rs190002721	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100332871	GTACAAGCTGTTTAT[A/G]TTTTGTGGAAATTAG	25897
rs190014154	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100322645	CTATCTCAGCTTTTG[C/G]CCTGCCTTCCTCATT	25897
rs190020321	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302030	CAGGAGGCCCTAATA[C/T]GGCTGAAAATTAATG	25897
rs190036970	snp	A/G	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100283890	AAAATCAAATATTCA[A/G]AAATTTACCAATATT	25897
rs190055747	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100324956	CTGTCACCCAGGCTG[C/G]AGTGCAATGGCACAA	25897
rs190090451	snp	C/T	0.0119091	0.0762411	intron-variant	RNF19A	GRCh38.p7	8:100285693	GCTGGAGTATAGTGG[C/T]GCAATCACGGCTCAC	25897
rs190175193	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278144	GGCATTCACTTTAGT[C/T]TGGCTTAGCCTCAGT	25897
rs190314114	snp	A/C	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100325576	CCCTCAGCAGCACCA[A/C]ACCTCTAGCCTACGC	25897
rs190373431	snp	C/T	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100293528	TGCTTGCATTCAACA[C/T]TGTTTTCTATCTTGG	25897
rs190475233	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100321102	AGGGTAGCTGTGGCG[G/T]TTTCTTAAAATAAGA	25897
rs190479433	snp	C/T	0.00517822	0.0506191	intron-variant	RNF19A	GRCh38.p7	8:100282733	CAGCATGTCAAAAGA[C/T]AGTCAAGGTATAGCT	25897
rs190614836	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275616	ATTTTATAAAAAACC[A/G]TATTAAATTAGTACA	25897
rs190651121	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100318549	TTAAATGTATACACA[A/G]AATAATTTCCACACT	25897
rs190673781	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100278205	TTGGCCTTTAGAATG[C/T]CAAATAAGCACATGG	25897
rs190686448	snp	C/T	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100298022	TAAGACTCAGTTTCT[C/T]CAATTATAAAATGTG	25897
rs190732572	snp	G/T			intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100300629	CTGTATTCCACCCTG[G/T]GTGACACAGTGAGGC	25897
rs190747301	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100260161	CTACTGCAGCACACT[A/G]CATAGTACCAGCCAT	25897
rs190938859	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100307518	TCTATATAAATCTAA[A/G]TAAGTGTTCAAGATA	25897
rs190945186	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336806	TCTGTTTCCTCCTTT[A/G]CTGCTAGGCCGTCAA	25897
rs190950261	snp	C/T	1.74397e-05	0.00295289	intron-variant	RNF19A	GRCh38.p7	8:100287498	CAAACATTATCTTCT[C/T]ACCCACAGTCTGGAG	25897
rs190951099	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100327397	GCTGGAATTACAGGC[A/G]TGTGCCACCATGCCC	25897
rs190965313	snp	A/G	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100268302	TGTTTGGACTTTCAC[A/G]AGATTGTTATAATTT	25897
rs190970195	snp	C/T	0.0138799	0.0821421	intron-variant	RNF19A	GRCh38.p7	8:100273896	CAAGTGATTCTCCTG[C/T]CTCACCTCCCGAGTA	25897
rs190972052	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100313433	GGAGGAACAGCAGAC[A/G]CAAAGGTCTTAGCCA	25897
rs191061898	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100333158	GTTTGTCACAAAAGT[C/G]TGTTTGGTCCTGTCT	25897
rs191090058	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100291385	TTGCTATTACTCTGT[C/G]ATCCTTAAGCCATAC	25897
rs191098083	snp	A/G	0.00597247	0.0543191	intron-variant	RNF19A	GRCh38.p7	8:100331761	CTCCTGCAGACAACT[A/G]TTATCCGTTTCATAT	25897
rs191106730	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100312371	CACTTTGAGAAGCAG[A/G]GGTGGTTGGATCACT	25897
rs191117727	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272781	TTTAGAACTTCTGAG[C/T]TCAAGCAATCTGGCC	25897
rs191126823	snp	C/T	3.29495e-05	0.00405877	missense, intron-variant	RNF19A	GRCh38.p7	8:100261713	CCAACACTTCCCTCC[C/T]CTATGCTTGGGTTGT	25897
rs191201776	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100292472	TGTGTGTGTGTGTAC[A/G]TATAAATTGTATTTG	25897
rs191209078	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100321900	CAGTGGCTTAAAATA[C/T]TCAGTAAACCATGCT	25897
rs191383223	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100267302	AGAGACCGAAATATC[A/G]AGGTTGCTGCAGGGT	25897
rs191450800	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100338035	CCAGGCTGTAGTGCA[A/G]TAGCACGATCTTGGC	25897
rs191489993	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297507	AGTGTGGCCACATTA[C/T]TAGTCCTGGCCAATG	25897
rs191521477	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267005	AACCTTATTCCCAGT[C/T]GGGTCCCAGAAGTTA	25897
rs191575604	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304353	ACAACTGCCTACCAG[A/G]TAACCACTGCCACCC	25897
rs191587135	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284766	TATTTTTATTAAGAA[A/G]TATCACATATAAAAA	25897
rs191592601	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100323250	GAAGGTAGTATTTCA[C/T]AGAAAGTTTTTAAGG	25897
rs191598145	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274496	TAAAATTTCATGTGA[C/T]TTTTTTTCTAGTAGC	25897
rs191598912	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100262871	CAGAATTTGCTGACA[A/G]ATCAATCAGATGTAG	25897
rs191639473	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287178	TAAACAAACCTGATC[A/T]TTTCATCTGTTATTC	25897
rs191683550	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100324085	TTACTACAGAGCTGT[A/G]ATTTTGAGATGACTT	25897
rs191688943	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305003	TACAGTGGCACAATC[A/T]CAGCTCACTGCAACC	25897
rs191767755	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306894	AAGTAAAGAAAAATT[C/T]AGCTATTCTCCGTAA	25897
rs191785714	snp	G/T	0.00318978	0.0398085	intron-variant	RNF19A	GRCh38.p7	8:100299763	AACTCTGTCTCAAAA[G/T]AAAAAAAAGAAAAAA	25897
rs191791081	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100328750	GCTGGCATTACAGGC[G/T]TGAGACACCGCACCT	25897
rs191805298	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258431	GCTGAACACAGAAAA[C/T]GTATCTGCATTATGA	25897
rs191813326	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280940	AAGACACTTGCTTTA[C/T]AGAAAATTCCAGGAG	25897
rs191822457	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307870	AAAATAGGAATCTTA[A/G]CACCTCTCGTGTGTT	25897
rs191923901	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100296129	TTTCTTTTTTGAGAC[A/G]GAGTCTCAATCTGTT	25897
rs192003241	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100323177	GCCCATAAATATTAG[C/G]TGTTACCCAGAGTGT	25897
rs192081540	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100327007	TCTGATTAACAGTTC[C/T]TCAGCAGATGTGTCA	25897
rs192225623	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100316324	AAAGAGCGAAAGAAC[A/G]AAGCTTCCACAGTGT	25897
rs192289051	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	RNF19A	GRCh38.p7	8:100256685	AGAATCTCTTAAAAT[A/G]GTCTTTTAAGATCTT	25897
rs192325101	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100303025	GTCTCTGATCATCAT[A/G]GCACATGATATAAAA	25897
rs192349005	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100262090	TAGGTCAGTAAGAAT[A/G]GGCTAAAAGTTGATT	25897
rs192350099	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329067	TCCAGGTGCCTCCAG[A/T]TCTGTCCTGGCTGCT	25897
rs192358801	snp	C/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310630	CCCAGAGGACGGCAG[C/G]ACCCTGTGCGTCTGC	25897
rs192390882	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289354	AAAATAAAAGACTGA[C/T]AAACTGGACTAGAAT	25897
rs192393193	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270262	GAACAAAGAATAAAA[A/G]AAGAATAAAAAGAGA	25897
rs192449739	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100315672	TGTTGTTGTTGTTGA[A/G]ACAAGGTCTCACTCT	25897
rs192474493	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275990	GTTTTTTTTTCCTTC[A/G]GATTAAAGACTGAGA	25897
rs192499822	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100314895	GAGAAAGAGGAAGCA[A/G]GCACAGAAGCTTAGC	25897
rs192519276	snp	C/T	0.00716266	0.059414	intron-variant	RNF19A	GRCh38.p7	8:100333790	GCCACTGCACTCCAG[C/T]CTGGGCAATAGAGTG	25897
rs192538548	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293390	CAGAACTCCAGGTTG[A/G]TATCTTTATCCTTTC	25897
rs192547939	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274895	CTTAACTTTAAAAAG[G/T]TAAAATAACTAGTGT	25897
rs192637134	snp	G/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100264386	TTCCCAGCCTTTCAG[G/T]TAATGCACATAAGGG	25897
rs192643709	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292879	AAACCTAATTGTTAC[A/G]TATTTACTTTCTGGT	25897
rs192718090	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320321	AAAACACTATTTTCA[A/G]GATCTACCCATGTTG	25897
rs192731127	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288633	TAGCTTACACAATCT[C/T]GCAGAACAAAGTAGG	25897
rs192783776	snp	A/T	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100293668	GAATTCGGGGAAAAT[A/T]ATTTCTTTAAGTATT	25897
rs192788885	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334730	GCTGGCGTGCACCCA[C/T]TCAGCACTTTCCTGT	25897
rs192860682	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100285276	TATTTATATAACCTA[C/T]ACCTCTGTAATCTGT	25897
rs192871058	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314071	ATTTTTTGTAGAGAC[A/C/G]AGGTTTTGCCATGTC	25897
rs192893594	snp	C/T	0.00438332	0.0466095	intron-variant	RNF19A	GRCh38.p7	8:100324961	ACCCAGGCTGGAGTG[C/T]AATGGCACAACCTCA	25897
rs192943422	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100268733	AATACTAAAAGAATA[C/T]ACCTAAAGATTTAGA	25897
rs192984194	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100309231	ATACTTCACCCCAAG[A/G]CTACACCATTTTGGT	25897
rs192985062	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269504	TAAACTAATGCAAAA[C/T]ATGCATATTTTTAGG	25897
rs193044555	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100298423	TAATTCAACTACTTA[C/T]AAATGAGGGAGATGG	25897
rs193064701	snp	C/T	0.00398564	0.0444627	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257092	TTTACATTTATTTAA[C/T]GTATGCAGTTTACAC	25897
rs193187891	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100328913	AATAGGACCCCCAGA[C/T]GACACAGCTAGAGCA	25897
rs193192092	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288916	ATACAAAAAACTAGC[C/T]GGGTGTGGTGGCGGG	25897
rs193230530	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100279647	AACGTCCGCCTCCCA[A/G]GTTCAAGCTCAGATT	25897
rs193258045	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100305462	TATGAATAAAAGTAC[A/G]TAAAGTCACTCATGA	25897
rs199534647	in-del	-/AAC	0.0036738	0.0427013	intron-variant	RNF19A	GRCh38.p7	8:100264224	AAATCAGTCATTACA[-/AAC]AACAACAACAAAATA	25897
rs199580684	snp	C/T	1.65625e-05	0.00287766	intron-variant	RNF19A	GRCh38.p7	8:100264639	AACTCCATAAAATTG[C/T]AGGTAATTAGTACTT	25897
rs199682255	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100296304	GAGACGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG	25897
rs199810141	in-del	-/T	0.00914312	0.0669923	intron-variant	RNF19A	GRCh38.p7	8:100282140	TCCAAAGCTACATTC[-/T]TTTAGTCAACTAATT	25897
rs199836732	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100274560	CAGGAATATAAATTA[G/T]TTTTAGTAGAGATGG	25897
rs199884829	in-del	-/A			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310771	TTTCATTTTTTTTTT[-/A]CTATTTTGCAGTCAA	25897
rs199908526	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100291950	ACTAGCACTGTTGAA[C/G]AGAAAGAGGACTAAG	25897
rs200083755	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100319921	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	25897
rs200127369	snp	A/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310761	ATCTCTTTTATTTCA[A/T]TTTTTTTTTACTATT	25897
rs200191120	in-del	-/TTT			intron-variant	RNF19A	GRCh38.p7	8:100267227	TCTCAGCTCTGCTTC[-/TTT]GTGTGTAACTGAAGA	25897
rs200236877	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100321991	GGTTTAGCAAAATTC[C/T]TTTTTTTTTCTTTAT	25897
rs200348503	in-del	-/CG			intron-variant	RNF19A	GRCh38.p7	8:100320727	AGATAAAATAATACA[-/CG]TAAAGCATTTAGCAC	25897
rs200458067	snp	C/T	9.8868e-05	0.00703024	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264714	CACGATTACAGACAA[C/T]GTTACACCACCTGCT	25897
rs200485009	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100274637	TGGTCGGCCCGCCTC[A/G]GCCTCCCAAAGTACT	25897
rs200523428	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100265582	CCCTCTGTTCCAAAA[A/C]AAATTCAAAACAGCC	25897
rs200555098	snp	A/C	1.72279e-05	0.0029349	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288151	ATTATATTTAGAGAT[A/C]AAACCTATTTCTTGT	25897
rs200579114	snp	A/G	8.27657e-05	0.00643242	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274975	TCCAGACTCTTGACT[A/G]TAACTAATGGATGAA	25897
rs200597199	in-del	-/AAG	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100312637	GGAGAGAAAGAAAGA[-/AAG]AAAACCGGGCGCAGT	25897
rs200598134	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100324901	TTTCTCTCTCTCTCT[C/T]TCTCTCTTTCTTTCT	25897
rs200711298	snp	A/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258851	CCATGACTACAAGAA[A/G]TTTTCATGCTTTCTA	25897
rs200805448	in-del	-/A			downstream-variant-500B	RNF19A	GRCh38.p7	8:100257029	ATTCTCATTCTTATT[-/A]AAAAAAAAACACTTG	25897
rs200857249	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100308808	TTCTAGCCAACATCT[A/G]GGTTTGAAAATTGCA	25897
rs200880822	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100276744	AAAAAAAAAAAAAAA[C/T]AAAAAAAGGAGTAAA	25897
rs200906445	in-del	-/A	0.00835141	0.0640778	intron-variant	RNF19A	GRCh38.p7	8:100298906	AGGAAAACCACAGGG[-/A]AAGCAGAGCGCAAAA	25897
rs200987506	in-del	-/AAAG			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311737	AAAAAAAAAAAAAAA[-/AAAG]AAAAGAAAATAGATC	25897
rs201085525	in-del	-/A	0.0111196	0.0737302	intron-variant	RNF19A	GRCh38.p7	8:100276309	TCTTCAGAGAATTAC[-/A]CCGAGTGAAAAAAGT	25897
rs201086737	in-del	-/TC			intron-variant	RNF19A	GRCh38.p7	8:100324827	CCTTCCTTCCTTCCT[-/TC]CTCCTTCTTCCTCCC	25897
rs201145151	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100294615	GCCAGTAAGACTCTT[-/G]ATTTTCTGCTTGACT	25897
rs201153762	snp	C/T	1.66888e-05	0.00288862	intron-variant	RNF19A	GRCh38.p7	8:100275172	CATATCTTGAAAGAA[C/T]AAGAAAAATGATTTA	25897
rs201209240	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100282249	TTGACTCATTAAAAC[A/C]CCACCAAAAATCTTA	25897
rs201246497	snp	C/G	0.000247735	0.0111268	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258769	ATGTGGGGAATTTTC[C/G]AGACGGTCATTTTCT	25897
rs201249163	snp	A/G	8.26713e-05	0.00642875	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264131	GACTCCACAACCTCC[A/G]CTTCGACAAAGAGAA	25897
rs201253948	in-del	-/A	0.0111196	0.0737302	intron-variant	RNF19A	GRCh38.p7	8:100323104	TTTGTAAACAAAAAC[-/A]AAAAAAACAAAAAAA	25897
rs201359077	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100294614	AGCCAGTAAGACTCT[G/T]GATTTTCTGCTTGAC	25897
rs201467304	in-del	-/C/TC			intron-variant	RNF19A	GRCh38.p7	8:100319311	GATGAAAGTTTTTTT[-/C/TC]CTTTTTTAACACAAA	25897
rs201527248	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288310	GATCATTTAATTGTA[C/T]TCTTAGTTTGTATAT	25897
rs201554011	snp	C/G/T	4.94368e-05	0.00497152	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288050	GAGGACTGAAGATCT[C/G/T]GATCTGAACCCATTT	25897
rs201558227	snp	A/C	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100295578	AATGAAAAAAGGGAA[A/C]TATCTGTCTTTGTGC	25897
rs201597779	in-del	-/A	0.0185938	0.0946107	intron-variant	RNF19A	GRCh38.p7	8:100272368	CTTCAGTGACTGGGG[-/A]AAAAAAACAACTAAT	25897
rs201658484	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268870	CCGACAGGAGCACCA[A/G]CCAGTGTTCCCAGTT	25897
rs201672696	in-del	-/A	0.00636936	0.0560724	intron-variant	RNF19A	GRCh38.p7	8:100296040	AATTGATTCCCCAAC[-/A]TAACTACCAAATTCG	25897
rs201688806	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100270511	AGCACTATGAATTTA[C/T]TTCTTCTAATTACAT	25897
rs201740699	in-del	-/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288380	CCATTAGTAGTAGTT[-/G]TTTTTTTTAACAAGG	25897
rs201783484	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307717	AAAATAGAGGTGACC[C/T]AAGTGTCTTACATCC	25897
rs201837276	snp	A/G	1.64817e-05	0.00287064	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258825	CAAAGCGGGTGTGAT[A/G]ATCACTGGAACCATG	25897
rs201957875	in-del	-/A	0.0260105	0.111035	intron-variant	RNF19A	GRCh38.p7	8:100308662	AAGAAAAGATATTTT[-/A]AAAAAAATGAAAAGA	25897
rs202024866	snp	A/G	3.29598e-05	0.00405941	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264702	TACTACTGGAGACAC[A/G]ATTACAGACAACGTT	25897
rs202025017	snp	C/T	0.000362337	0.013455	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259013	TCCTCTCTCGTCTCA[C/T]TTATCTTCATGTTAC	25897
rs202138277	in-del	-/AGAA	0.0126979	0.078662	intron-variant	RNF19A	GRCh38.p7	8:100312626	GAAGGAGGGAGGGAG[-/AGAA]AGAAAGAAAGAAAAC	25897
rs202182583	snp	A/G	0.00199792	0.0315431	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258552	TTCTGCAGCATTTAT[A/G]GGCCTAAATTTCAGT	25897
rs267601677	snp	A/G	3.295e-05	0.00405881	RNF19A	8	allele_origin=G(germline)/A(somatic)	8:100287967	TTTTCCTCCGAAACA[A/G]GGAGCCTATTGAAAT	25897
rs367566529	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100284466	CTTTTTTTCCTCTGT[C/T]CTTTGTGGGTAAGAC	25897
rs367600432	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100295239	GACATACATATATGG[C/T]AGTCCCATAACTGAA	25897
rs367633977	in-del	-/AATAT			intron-variant	RNF19A	GRCh38.p7	8:100282514	GCTATTAACTCTTAT[-/AATAT]GTTTATGTATGTGTG	25897
rs367638112	snp	C/G	3.295e-05	0.00405881	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258899	TCAGAAAAATGACTA[C/G]AGTGAGAATCTGCTA	25897
rs367676625	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100322001	AATTCTTTTTTTTTT[C/T]TTTATCAATACCCTG	25897
rs367760896	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293292	TGATATGCAGGTCTC[C/T]TAGCAATGAATTCTT	25897
rs367899691	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100334971	GGGTTAAAATAAGCT[C/T]AGATCTCCCCAAACA	25897
rs367903524	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100292200	TATGTTGAGAAGATA[A/G]TAAAGAATAAAAAAA	25897
rs367983580	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100278634	GCAAATAAGTATTTA[C/T]AAAAATATACAAGGC	25897
rs368066114	snp	A/G	3.29946e-05	0.00406155	stop-gained, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258702	CAATATGATTCAACT[A/G]TGAAACTTCTGAACA	25897
rs368130176	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317056	ACCAGCAGCGCTGCC[C/T]GGCTACTCTGAGTGC	25897
rs368175628	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100332174	CTTTCCATACTGATA[C/T]CTGATTTGGTTTGGC	25897
rs368228376	in-del	-/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311740	AAAAAAAAAAAAAAA[-/G]AAAAGAAAATAGATC	25897
rs368230261	snp	A/G	3.29636e-05	0.00405964	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268869	TCCGACAGGAGCACC[A/G]ACCAGTGTTCCCAGT	25897
rs368321690	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100329827	CTAGATTTCAGCTCA[A/G]TGAAAAGCAGACATT	25897
rs368375252	snp	C/T	0.000153988	0.00877328	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288117	TTGAGACAGGGTCAG[C/T]GTTTACACACAGCCC	25897
rs368378560	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316267	TTACAGCTCATAAAA[A/G]CAGCGTGGACCCAAA	25897
rs368393150	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100271266	AGCCAGACCAGGACA[A/G]TTGATAATTACTAGA	25897
rs368402617	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297875	AGGTTTTTTAAATGC[C/T]ATATAAATATGGGGT	25897
rs368423268	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100312655	AAAACCGGGCGCAGT[G/T]GCTCACGCCTGTAAT	25897
rs368425916	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100286407	ATAATATCTGAATCC[G/T]ACATACAACTAATTC	25897
rs368459412	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100282601	GTAGTTTATTCATTA[C/T]GGCTCTTTATACCCT	25897
rs368463254	in-del	-/CTTTT			intron-variant	RNF19A	GRCh38.p7	8:100287425	CATGTAAAAATTTTT[-/CTTTT]GAGTAATAGCAAATT	25897
rs368479522	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289224	TGGATGGCTCACCCA[C/T]GTGTGAAAATCAATT	25897
rs368515029	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257448	CATTGTCCATAAACA[A/G]AAGCAAAAGAAAATA	25897
rs368580933	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100272538	CCAAGTTCACTACAC[-/T]TTTTTTTTTTTTTTA	25897
rs368674411	snp	A/C			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304497	ACCAGTTCCCACCCC[A/C]ACTTACGCACTCACA	25897
rs368674512	snp	C/T	0.000164728	0.00907398	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258986	TGTTGTTCTAACAAC[C/T]GTGCATCCATGTCCT	25897
rs368692505	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100321009	CAGCAAGTCAAAGAC[A/G]TAATCTTTTTGCTGG	25897
rs368731772	in-del	-/T	0.00318978	0.0398085	intron-variant	RNF19A	GRCh38.p7	8:100326476	GTGCTGGGCAGAGGG[-/T]ATTATACTAGAGACA	25897
rs368751554	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100299481	ATTAAGTGTTTGGAC[C/T]GGGTGCGGTGGCTCA	25897
rs368794942	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100265262	AGTTCTAATAAACAA[A/G]TATGAATAAACAGTA	25897
rs368817449	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100317443	GAGTGCCAGGGGAAA[A/G]GAAATTGTTTCTTCC	25897
rs368857214	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100327245	ATTCAGCAATTACTT[C/T]TTTTTTTTTTTTTTT	25897
rs368869015	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257701	AAGACATGGAAAACA[A/C]CACAGCAAAATCCTC	25897
rs368908675	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291674	CAGAAAACACTTACT[C/T]CCCAAGAGGAAAACC	25897
rs368980254	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100266648	CCTTAATAGCGGGGG[C/T]TACAGGCATGCACCA	25897
rs369113559	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100308670	GATATTTTAAAAAAA[A/T]GAAAAGAACCATGTT	25897
rs369142366	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100307571	AACCGTGGTGGGGAG[A/G]GGGTGTCAGAATCTT	25897
rs369215700	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337836	GCACCTGGAGTTAGA[C/T]TATCTAGTCTAGTAA	25897
rs369226277	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100322244	TTGTTTAGTATAGTC[C/G]CTTTTATTAATGATC	25897
rs369240999	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100308304	GAGAACATTAAGCAG[A/G]GCATTAAACTAACAA	25897
rs369249941	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100324481	AACAATGGATTCCCT[A/T]GAAATACTACATTTT	25897
rs369309048	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100333080	CCATTTCTAGTATGG[-/A]AAAAAAAAAAGAACA	25897
rs369317315	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100282924	TCATAGCAAACCAGC[C/T]TGAAGCTTACACAAA	25897
rs369321921	snp	G/T	1.69573e-05	0.00291177	intron-variant	RNF19A	GRCh38.p7	8:100270030	TATTGGGAACACAGA[G/T]AAATCTATTAAGTAC	25897
rs369324395	in-del	-/CCCAGCCCGGGTTC/CCGCACGCAGCCCAGCCCGGGTTC	0.430434	0.173042	intron-variant	RNF19A	GRCh38.p7	8:100317127	GCTGGCCCGCAAGCG[lengthTooLong]CCGCACGCAGCCCAG	25897
rs369352344	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100301405	ACAAATTTCCACTGG[C/T]TTCCCCGAGATGAAG	25897
rs369364210	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100260466	TTAGAGACAGGGTCT[C/T]GTTATGTTGCCCAGG	25897
rs369453714	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100290414	GCCAAACTTTCTTAA[C/T]ATGTGCAGTATGCAT	25897
rs369507392	snp	A/G	0.000131837	0.00811795	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275116	GCCCTCTCGCCCACA[A/G]GTTAATTTTGGACAG	25897
rs369550229	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289994	CTACACACAAGACAG[A/G]ACTCTCATACAAAAG	25897
rs369572250	snp	C/T	0.00438332	0.0466095	intron-variant	RNF19A	GRCh38.p7	8:100330934	CTCTGAGCTGGTCTT[C/T]CTGAAATCTGACTCC	25897
rs369687244	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100260609	TAGTATATACCACTA[C/T]AACTTAAGAGTTTGT	25897
rs369703632	snp	A/C			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289603	CATTCAGAGACAACA[A/C]ACCTAATAGGATGGC	25897
rs369720462	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100261396	AGCCACTGCACCTGG[C/T]CCCAAATTTCATTTT	25897
rs369734737	in-del	-/GCCT			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305180	TCAAATGATCTGCCT[-/GCCT]CAGCTCCCCATACTG	25897
rs369862688	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100327426	CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG	25897
rs369970301	snp	A/G	0.000153988	0.00877328	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275083	CTGTTTACAGTGGTA[A/G]CAAAACTCTGTTCCA	25897
rs369971691	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100285272	CTTTTATTTATATAA[A/C]CTACACCTCTGTAAT	25897
rs370011024	in-del	-/AT/TA	0	0	intron-variant	RNF19A	GRCh38.p7	8:100296589	ATGTTAATTTGTGAA[-/AT/TA]TATATATATATTCTA	25897
rs370046738	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100267115	AACAGAATGGATTGC[C/T]TCATGAGTTGGTGGT	25897
rs370155023	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100300872	CAAAGAGTGAAAAGG[C/T]TACAAATTCTGGACC	25897
rs370200609	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328684	ACCATGTTGGTCAGG[A/C]TAGTCTCAAACTCCT	25897
rs370210847	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337168	AATCTCTGGTTCTGA[A/G]GAATCAAAACATACT	25897
rs370226698	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100286129	CAAGGGCGATTCAAT[C/G]GCATCTAAGCTGTTT	25897
rs370291571	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100275648	TATTGTATGCACACA[A/C]AAAAAAGACTAGAAG	25897
rs370337630	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100271969	TTGGCTAAGCTTTCA[C/T]CTTCTGTATCTTTTT	25897
rs370420140	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100330870	AACCCTCTTGAGACT[A/C]TTGCTGTGTATACAG	25897
rs370482291	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310758	TTCATCTCTTTTATT[C/T]CATTTTTTTTTTACT	25897
rs370496881	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100266690	TGATTATTTAGTTTT[C/T]TGTAGAGACAAGGTG	25897
rs370604708	snp	A/T	1.64789e-05	0.0028704	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287586	CGTATTTTTCCATCA[A/T]GACATCATCACTTAA	25897
rs370677332	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100278070	ACCACTTAATACTTG[A/T]GTAATTTTAAGTAAA	25897
rs370677769	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100290935	TCCTGCCAGTGCCTC[A/G]CACTGGGTAAATCCA	25897
rs370698898	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100273649	ATGATAGCCCAGACA[C/T]ACTTAAATCTCTAGA	25897
rs370727679	in-del	-/CT	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100271870	ATGAAATTGTTTATG[-/CT]GTTAGTTGATCCCCC	25897
rs370795166	snp	C/T	3.3054e-05	0.00406521	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258614	TGTGAGTGGTTGTTA[C/T]TTGTTTCTTTTAGTG	25897
rs370797983	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100263186	GAGAACTGAGCTCTG[A/G]GGAACAAACATTTAG	25897
rs370841438	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258965	AATTCACTTGAGTTC[A/G]TGCTTTGTTGTTCTA	25897
rs370891135	in-del	-/GAGT			intron-variant	RNF19A	GRCh38.p7	8:100332320	CTCATGATAGTGAGT[-/GAGT]TCTCACGTGATCTGA	25897
rs370917188	in-del	-/CCAAA			intron-variant	RNF19A	GRCh38.p7	8:100261533	CCAAACCAAACCAAA[-/CCAAA]ACACACACCTGTTAA	25897
rs371007002	in-del	-/A			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303937	TGAAACTCTGTCTCC[-/A]AAAAAAAAGTTTTTA	25897
rs371076403	in-del	-/GCT			cds-indel, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257355	CATTGAGGTTAACCT[-/GCT]TTTATTTAAGTGAAT	25897
rs371157088	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291400	GATCCTTAAGCCATA[C/T]GGCCTTACTACATCC	25897
rs371171725	snp	C/T	6.58957e-05	0.00573964	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287882	GTACACATTTCAGAA[C/T]GTATACTTTCAATAC	25897
rs371175005	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100265066	AATCAAAAGTAGTGT[A/G]ATTATGTATCGAGCA	25897
rs371182615	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293154	GCTCGCCTCCTGCTG[C/T]GTGGCCCAGTTCCTA	25897
rs371251926	snp	C/G	3.29489e-05	0.00405874	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287865	AAATGGAGTTCTTAT[C/G]AGTACACATTTCAGA	25897
rs371265748	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100331027	CCTTTCACATTGATA[C/T]GTCCATTTCTATCTA	25897
rs371271506	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100332001	CATATATTAACTAAA[C/T]AATTTCCTATTGGTA	25897
rs371272682	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100279705	ATTTTTTTTGTATCT[C/T]TAGTAGACACGGGGT	25897
rs371291342	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100260545	AAAGTGCTGGGATTA[C/T]AGGTATGAGCCACTG	25897
rs371302041	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100292435	GCTTGCTATCATATG[G/T]GTGTGTGTGTGTGTG	25897
rs371385291	in-del	-/TTTTTTTTTTTTT			intron-variant	RNF19A	GRCh38.p7	8:100313903	GAGAAAGAGAACTAC[-/TTTTTTTTTTTTT]TTTTTTTTTGAGACA	25897
rs371393884	snp	A/G	1.65452e-05	0.00287616	intron-variant	RNF19A	GRCh38.p7	8:100261526	AAGCAGAACCAAACC[A/G]AACCAAAACACACAC	25897
rs371427106	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100293595	GTTTTCCTTGTCTCT[A/G]TCCTGCTTGGGGTTC	25897
rs371438033	snp	A/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274958	ACATAAATACCTGCT[A/G]CTCCAGACTCTTGAC	25897
rs371546324	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100272648	GGTCAAGCAATCCTC[C/T]ACTTCAATCTCCCAA	25897
rs371576680	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100333516	GCGAGATCAGTACCA[C/T]ATAAAAGTATATCAA	25897
rs371605593	snp	A/G	0.00358779	0.0422022	intron-variant	RNF19A	GRCh38.p7	8:100260310	CTTTGTAATGTTTCA[A/G]TGCAAAACACAAAGT	25897
rs371765541	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100283146	AAATGTTCTTGTATA[G/T]TCAAAGCTCCCCAGC	25897
rs371795753	snp	A/G	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100272725	ATTTTTGTATTTTTA[A/G]TAGAGACGGGATTTC	25897
rs371991316	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317089	GGCCTGCCAAGCCCA[A/C/T]GCCCACGCCCACCCG	25897
rs372006664	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100293681	TTATTTCTTTAAGTA[-/T]TTTTTTACCACACTG	25897
rs372106074	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100313519	AGTATGACGTGGGCC[A/G]GGGGACGGGGGGTGG	25897
rs372161844	snp	C/T	0.000367546	0.0135515	intron-variant	RNF19A	GRCh38.p7	8:100268952	ATCCTGATGGACTAA[C/T]GGAAAAAATTATAAT	25897
rs372212716	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100327376	CATGCCTCAGCCTCC[C/T]GAGTAGCTGGAATTA	25897
rs372307177	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100313525	ACGTGGGCCAGGGGA[C/G]GGGGGGTGGTCAGAA	25897
rs372308286	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307754	GCAAACATACTGCTT[C/T]ACGACTTCACTTACA	25897
rs372312831	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100284563	TTTATATAATAATCA[C/T]GTGGTTGTTTTCATA	25897
rs372316956	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100274599	CACGTAGCCCAGGCC[A/G]TTCTCGAACTCCTGG	25897
rs372352486	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280654	AAAAGTTAGAGCAGT[C/T]TGTCTAGTAGTTTTT	25897
rs372430260	snp	C/T	0.00398564	0.0444627	intron-variant	RNF19A	GRCh38.p7	8:100265334	AAATGACTCAAATTC[C/T]AGGGCTCTCATTTAT	25897
rs372442795	in-del	-/AT			intron-variant	RNF19A	GRCh38.p7	8:100319145	GACTCAAAGATGGAC[-/AT]TCTATGGATGGTTTA	25897
rs372546586	snp	A/G	0.000191683	0.00978799	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288197	AAGTCATGATGTAAG[A/G]ATATCCTACTTGGTT	25897
rs372621404	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326379	CCAGCATTTTCCATT[C/T]TTCTAAGTCCCTAAT	25897
rs372649024	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100323112	ACAAAAACAAAAAAA[A/C]AAAAAAAACTGTGAA	25897
rs372651567	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100297112	TTACCACTGAAAAAA[-/A]TTTTAAAGTTGATTA	25897
rs372679003	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100309272	ATTTTTGCTTTTGAA[A/G]GAGGTGGTAGCAGTC	25897
rs372713479	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100269849	CATTTACATATAAAT[A/T]GCTCCTTCTATAAGC	25897
rs372734358	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100334695	TTCATTGAGTCCCAC[C/T]CCTTTCAAGACCCAG	25897
rs372753678	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100291967	AAAGAGGACTAAGTC[-/T]TTTTTTTTTTTTTTT	25897
rs372756717	in-del	-/A	0.0111196	0.0737302	intron-variant	RNF19A	GRCh38.p7	8:100323112	CAAAAACAAAAAAAC[-/A]AAAAAAAACTGTGAA	25897
rs372771127	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100328990	CTGGGTCTTGCGCAG[G/T]TTTATCAGTTTGGCT	25897
rs372796082	in-del	-/ATGGCCTTAGCCA			intron-variant	RNF19A	GRCh38.p7	8:100283235	TTAGCCAACTGAAAC[-/ATGGCCTTAGCCA]AGGTGATAGAAACTA	25897
rs372896846	snp	A/C	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258951	GGGATGGAGCCTCAA[A/C]TTCACTTGAGTTCGT	25897
rs372957685	snp	A/G	0.00398564	0.0444627	intron-variant	RNF19A	GRCh38.p7	8:100276347	AAAATGTTACATACT[A/G]TATGATTCCATTTAT	25897
rs372969174	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100322125	AAGGAGAGAGTCAGC[C/G]TCTCCTTTGAAGCTT	25897
rs372979190	snp	A/G	1.65679e-05	0.00287814	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275158	AAATGCTATCACAGC[A/G]TATCTTGAAAGAACA	25897
rs373024531	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100334155	CCACCTTCTCCATCT[C/T]GACTTTCACCTTGCC	25897
rs373138369	in-del	-/C			intron-variant	RNF19A	GRCh38.p7	8:100291967	GAAAGAGGACTAAGT[-/C]TTTTTTTTTTTTTTT	25897
rs373196488	snp	C/T	1.65045e-05	0.00287263	missense, intron-variant	RNF19A	GRCh38.p7	8:100261551	ACACACCTGTTAAAA[C/T]AGTTTACCATGGCAC	25897
rs373229696	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100262060	AGGGTGTCATTTAAA[G/T]AGCTTATTATTCTCT	25897
rs373303122	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100292266	GAGATTGGGAATCCA[C/T]GAGGAACATTTGCTT	25897
rs373477661	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100276771	TAAAATGAGGGATCT[C/T]TGTTGTGATGGAACT	25897
rs373481848	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100331866	TACACAGTACTAACC[G/T]TTGCACCCTGCTTTT	25897
rs373484394	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100330561	AGTTGCCAGAAGCCA[A/G]CATGTGGAAAGAGTC	25897
rs373516184	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289615	ACACACCTAATAGGA[C/T]GGCTAAAATTAAAAG	25897
rs373523222	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100273730	TACTATGAGCCAGGA[A/G]CTATTTCAACTATAT	25897
rs373580322	snp	C/T	6.59424e-05	0.00574168	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259950	ACTGTGCCAGATTCT[C/T]CACTTAGACTGTACC	25897
rs373620164	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100267574	GGGGTCTCACTATGT[C/T]GTCCAGGCTGGTCTT	25897
rs373732744	snp	C/T	0.000153988	0.00877328	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287723	ACACAAGATCTGTGA[C/T]GACAAGTCATTATAT	25897
rs373748309	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323279	GGAAGAAAGAAAACT[A/T]TATTCTTCTCTGTAA	25897
rs373796452	snp	A/G	3.30349e-05	0.00406403	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258774	GGGAATTTTCCAGAC[A/G]GTCATTTTCTACCTC	25897
rs373944861	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100320657	TAGGCCTGTTTTCTC[A/G]TTTTTATAATGAAGG	25897
rs373959438	snp	G/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100272215	CCAAGTGCCTAAACC[G/T]CCTAGTAGCTATAAA	25897
rs373967017	snp	A/G	1.71867e-05	0.00293139	intron-variant	RNF19A	GRCh38.p7	8:100263998	CTACTTACACTGTTA[A/G]TAAGCACATTTTCTT	25897
rs374026224	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100276744	AAAAAAAAAAAAAAA[-/G]AAAAAAAGGAGTAAA	25897
rs374035801	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285970	TATTTGTTATAATGA[C/T]TCACAAAAAGTTTTT	25897
rs374084512	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100282998	GTTAGTAGCATACAG[C/T]CAGGCTGGTTCATTG	25897
rs374111480	snp	G/T	1.71484e-05	0.00292812	intron-variant	RNF19A	GRCh38.p7	8:100268737	CTAAAAGAATACACC[G/T]AAAGATTTAGAATAA	25897
rs374130728	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100279697	CTTGGCTAATTTTTT[C/T]TGTATCTTTAGTAGA	25897
rs374144598	snp	A/G			missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258713	AACTGTGAAACTTCT[A/G]AACAGGAAGCAGTTT	25897
rs374226392	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100259344	AAATTCAGACTATAT[A/G]TAAGCTATGAGAACA	25897
rs374228079	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100321583	GATATTTTGAACGCT[G/T]CCCATGAATGACAAA	25897
rs374345505	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310415	TCTCCGTGGCCCAGA[A/G]AGCGTCTCCTCCAAG	25897
rs374425898	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304486	TCACACTACTTACCA[G/T]TTCCCACCCCCACTT	25897
rs374513804	snp	A/G	0.000153988	0.00877328	intron-variant	RNF19A	GRCh38.p7	8:100259830	TAAAAAATACTTTCA[A/G]TTTTTTAACAGTTTT	25897
rs374552138	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288765	AAAAAGTAGTCAAGA[A/G]AAAGTCCCATATAGG	25897
rs374665926	snp	A/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100312090	CCAGAAACCTAGGAT[A/T]GTTCCCAGGCCCCAT	25897
rs374671565	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100335815	TGCCCACAGTCCCTG[C/T]GGAGGTGCGGGCCTA	25897
rs374675154	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291090	TATAAAGAAGAGAAC[C/T]TGGGAGTCAAAAGAC	25897
rs374694444	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100325592	ACCTCTAGCCTACGC[C/G]CTGGGTCCTCAAGCC	25897
rs374747875	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100331286	TGTAGAAAAGCCATC[A/G]TCCTCTTGAGATATT	25897
rs374761999	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100260608	GTAGTATATACCACT[A/G]TAACTTAAGAGTTTG	25897
rs374764719	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100317104	CGCCCACGCCCACCC[A/G]GAACTCCAGCTGGCC	25897
rs374766252	snp	A/C	0.00716266	0.059414	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289303	ACTATTTCTATGAAA[A/C]AATTCTTAAACAGAA	25897
rs374825869	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100312953	CAACAACAACAAAAA[-/T]AAATACATAACCTCT	25897
rs374851551	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100328253	TCCCAGACCCTCAAG[C/G]TACTTAGGACCTCGT	25897
rs374944361	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100319149	CAAAGATGGACATTC[G/T]ATGGATGGTTTACTA	25897
rs375000162	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100328807	AATGGTTGTGCAAAT[C/G]TTAGATCAGGGAGAT	25897
rs375005003	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100271151	TCTTCTAGGACCAAA[C/G]ATGCTTTTTTTTTTT	25897
rs375014597	snp	C/T	0.000181367	0.00952106	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258633	TTTCTTTTAGTGCAT[C/T]GCCAAAATATAAATC	25897
rs375036606	in-del	-/AAGA	0.00120192	0.024485	intron-variant	RNF19A	GRCh38.p7	8:100323266	AGAAAGTTTTTAAGG[-/AAGA]AAGAAAACTTTATTC	25897
rs375071810	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100287015	GCAAATGCTTATGTA[C/T]ATCAACATGAACACA	25897
rs375156052	in-del	-/ACGCAGCCCAGCCCGGGTTCCCGC			intron-variant	RNF19A	GRCh38.p7	8:100317155	AGCCCGGGTTCCCGC[-/ACGCAGCCCAGCCCGGGTTCCCGC]TCGCGCCTCTCCCTC	25897
rs375191840	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100334743	CATTCAGCACTTTCC[C/T]GTCTGGTTTCCAGGC	25897
rs375236548	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100299643	ACATGCCTTTAATCC[C/T]AGCTACTCGGGAAGC	25897
rs375240233	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100330404	AAAGTCATGACCTGT[A/G]AGGGTTATGATCTTT	25897
rs375274061	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100319548	TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT	25897
rs375355995	in-del	-/C	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310976	TCCTCCTGGTTTATT[-/C]TCTTCAAGATTTAGA	25897
rs375383834	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100282524	CTTATAATATGTTTA[C/T]GTATGTGTGTTCTAA	25897
rs375575301	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100280024	CTATCTTAAAGCACT[A/G]TTATCTCTATACTCC	25897
rs375701691	in-del	-/TCCT			intron-variant	RNF19A	GRCh38.p7	8:100324827	CCTTCCTTCCTTCCT[-/TCCT]CCTTCTTCCTCCCTC	25897
rs375748151	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283498	CAAATTTGGTCCCCT[A/G]GGCCCCTCCTCAAGT	25897
rs375762328	snp	A/C	0.00358779	0.0422022	intron-variant	RNF19A	GRCh38.p7	8:100326579	CCTGCTTTACTGATA[A/C]CATTCAATAAAGGGG	25897
rs375795636	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293597	TTTCCTTGTCTCTAT[C/G]CTGCTTGGGGTTCAC	25897
rs375820113	snp	C/T	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100272869	CTGCATTTCTAATTC[C/T]TCCTCTTGTTTTTGG	25897
rs375821399	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100268597	AAGTCTGCTTTATAC[-/G]TATTTATATATGCTT	25897
rs375948413	snp	C/T	0.00597247	0.0543191	intron-variant	RNF19A	GRCh38.p7	8:100305418	AAGAAACATGTCATA[C/T]AAAACGCCCCTAGAG	25897
rs375962198	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100299096	CTTACTGTGTCCCTT[C/G]GTTCTCAACAGAAGG	25897
rs375974753	snp	A/G	0.000153988	0.00877328	intron-variant	RNF19A	GRCh38.p7	8:100275197	GATTTAAAATGTGAC[A/G]TAAAACAAGAGATAC	25897
rs375987830	snp	C/G	0.000122046	0.00781076	intron-variant	RNF19A	GRCh38.p7	8:100259258	TTCTCTGAAATATAA[C/G]AGTAACAAATACAAA	25897
rs376029440	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100306616	AGTATCACTGACATA[C/T]GATAACTTTTGAGAA	25897
rs376046271	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100260315	TAATGTTTCAATGCA[A/G]AACACAAAGTTAGAA	25897
rs376049627	snp	A/C	1.64741e-05	0.00286998	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287913	TTGCAATTCCATCCA[A/C]CCCGCCATTTAGCTC	25897
rs376058492	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100313809	GTGGAGACAGAAGTG[A/G]ATGGTTTTGGTTTTG	25897
rs376139217	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100259484	TCTAGACACTATGCT[A/G]CCTTTTTTTAAAGAA	25897
rs376139332	snp	C/T	1.66857e-05	0.00288835	intron-variant	RNF19A	GRCh38.p7	8:100261506	AATAATTTGTAGTTA[C/T]CAGAAAGCAGAACCA	25897
rs376159826	snp	A/G	0.000214293	0.0103489	synonymous-codon, intron-variant	RNF19A	GRCh38.p7	8:100261613	AGCTAGTGCCATGGT[A/G]CTGGCCGTTTCACTC	25897
rs376226880	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316587	CTAGATACAGAGCGT[C/T]GATTGGTGCACTCAC	25897
rs376267132	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100327895	CAAATATATCATTTC[G/T]TTATTACTGTTGACA	25897
rs376332157	snp	C/T	3.29527e-05	0.00405898	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259131	AGCCACTGGATGAAC[C/T]GCCAGCATGACTTCG	25897
rs376336797	in-del	-/AATCTAA			intron-variant	RNF19A	GRCh38.p7	8:100302178	ACAGAGATAGTTTAA[-/AATCTAA]GTTTAAAAGGATCAT	25897
rs376425857	snp	A/C/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100284231	GGATAGGGACTCAAA[A/C/G]TCAGGTATTTACAGC	25897
rs376431058	snp	C/T			intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309559	CGCCGGCCGCACAGG[C/T]ACCAGGAGGACAGGG	25897
rs376486658	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100294663	ACATAGACTTTTCTT[C/T]AGGGGGAAAGATGTA	25897
rs376493290	snp	A/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337562	GACTGCCCCTAGTCA[A/T]ATTAGCTGGTCAGAG	25897
rs376583936	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100312098	CTAGGATTGTTCCCA[C/G]GCCCCATTCTTTTTG	25897
rs376603364	in-del	-/AT			intron-variant	RNF19A	GRCh38.p7	8:100271645	ATGCTAAAATCACAC[-/AT]GAGAATTAATACCAC	25897
rs376646475	snp	G/T	1.64898e-05	0.00287135	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259987	TCTGTACATCTGCTT[G/T]TACTTCCAACCTTAA	25897
rs376757415	in-del	-/CAT			intron-variant	RNF19A	GRCh38.p7	8:100265472	AGAATTTGATATCAT[-/CAT]AGAAGCGGTGATTAA	25897
rs376833239	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100321732	GAAAGTTGAAATTAC[G/T]CTTTCATCCATGGGC	25897
rs376850005	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100322229	TATATTGAAAATCTG[C/T]TGTTTAGTATAGTCC	25897
rs376881086	snp	G/T	1.80052e-05	0.00300038	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258520	CAGCTCCAAACACGG[G/T]TGTACAGTGGTAATT	25897
rs376906759	snp	C/T	4.9423e-05	0.00497082	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287870	GAGTTCTTATCAGTA[C/T]ACATTTCAGAATGTA	25897
rs376918012	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285740	TGGGTTCAAGTTACC[C/T]TCCCGTCTTGGCCTC	25897
rs376971505	snp	A/G	0.000153988	0.00877328	intron-variant	RNF19A	GRCh38.p7	8:100261502	AATTAATAATTTGTA[A/G]TTACCAGAAAGCAGA	25897
rs376994568	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100302389	CTGATTAATCAGAAG[C/G]CTGAAACTGCTATCA	25897
rs377017421	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100274663	GTACTGGGATTACAG[A/G]AGTGAGCTACCATAC	25897
rs377092771	snp	A/C	0.00478085	0.0486577	intron-variant	RNF19A	GRCh38.p7	8:100307416	ACTACATATCTCAAC[A/C]ATCTGTGCCCTGTAG	25897
rs377100325	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100325442	CTGGCCAGTTTCATG[A/G]TCTCTGATGCTGGTG	25897
rs377160499	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100316170	AGCTCTTAAGACGGC[A/G]TGTCTGGAGTTGTTC	25897
rs377216732	snp	C/G	1.64996e-05	0.0028722	intron-variant	RNF19A	GRCh38.p7	8:100260004	ACTTCCAACCTTAAA[C/G]GGGGGTATGAAATCA	25897
rs377232407	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100285993	AAGTTTTTTTAAAAC[G/T]AAAATTTGCTATCCT	25897
rs377277282	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100318207	CCTTGTTTATTATCC[C/G]CATTTGTTTTTGCCT	25897
rs377282678	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289655	TCCAAGTGTTAGCAA[G/T]GATGTGGAAGAATAG	25897
rs377346318	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100269221	GTTAAAAATTTATCC[C/T]TAGTCTTCCATTACC	25897
rs377389531	snp	C/G	1.66977e-05	0.00288939	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258595	TTTTAATTCCATTGT[C/G]TGATGTGAGTGGTTG	25897
rs377429903	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316808	GGTCTGTGGGATTGG[C/G]TGCCGTGGAGCAGGG	25897
rs377436690	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100334233	AATGCTTCACGGTTC[C/T]GCCACCATTTCTTGT	25897
rs377481976	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270689	TCATATGGCTATGAA[C/T]GTTATAAACCATGGA	25897
rs377527930	snp	C/T	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100302292	TGAGAAAGATGACGA[C/T]GGCACATCAGTGAAG	25897
rs386413474	in-del	-/TGGCCTTAGCCAACTGAAACA			intron-variant	RNF19A	GRCh38.p7	8:100283216	CGCTGGTAGCAGGGT[-/TGGCCTTAGCCAACTGAAACA]GGCCTTAGCCAACTG	25897
rs386413475	in-del	-/CT			intron-variant	RNF19A	GRCh38.p7	8:100324899	CTTTCTCTCTCTCTC[-/CT]TTTCTCTCTTTCTTT	25897
rs386728191	in-del	AG/GGC			intron-variant	RNF19A	GRCh38.p7	8:100272846	TAAGCCACTGCGCCC[AG/GGC]CCCTCACTGCATTTC	25897
rs386728192	in-del	C/TTAGGA			intron-variant	RNF19A	GRCh38.p7	8:100314369	CCTAAAGCTCCCAAA[C/TTAGGA]TCTGAGGCACAAGAG	25897
rs386728193	multinucleotide-polymorphism	ATAACAATGAAGTTTGCCACATCA/GTAACAATGAAGTTTGCCACATCG			intron-variant	RNF19A	GRCh38.p7	8:100321117	GTTTCTTAAAATAAG[lengthTooLong]ATTGACTCTTCCTTC	25897
rs386728194	multinucleotide-polymorphism	ATA/GTG			intron-variant	RNF19A	GRCh38.p7	8:100334589	CCTTCTCCCTTTCTT[ATA/GTG]CCCCACCTCCGAGCT	25897
rs397933826	in-del	-/TGGCCTTAGCCAACTGAAACA			intron-variant	RNF19A	GRCh38.p7	8:100283236	TAGCCAACTGAAACA[-/TGGCCTTAGCCAACTGAAACA]GGTGATAGAAACTAA	25897
rs397959002	in-del	-/CA			intron-variant	RNF19A	GRCh38.p7	8:100325783	ACACACACACACACA[-/CA]TTTATATCCATAAAA	25897
rs397963093	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100298212	TAAAAAAAAAAAAAA[-/A]CACTTATTACACATT	25897
rs397974168	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100308701	TTTAAAAAAAAAAAA[-/A]TGTGGAATGTAAAGA	25897
rs398112802	in-del	-/C			intron-variant	RNF19A	GRCh38.p7	8:100272850	CACTGCGCCCAGCCC[-/C]TCACTGCATTTCTAA	25897
rs398112803	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100296179	CATAATCTCAGCTCA[-/A]CTGCAACCTCTGCCT	25897
rs527288851	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100281336	TTAAAGTGGTTTTTG[C/T]TTTCTATTATAGGAT	25897
rs527384451	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303623	GGATATTTAACGTTT[A/G]TGCATAATTTTAAAA	25897
rs527390555	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100299081	AACAGACACATTTTG[C/T]TTACTGTGTCCCTTG	25897
rs527450225	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334640	AAGATGGGACCAGCA[C/T]TGGTATGTTTTCTAA	25897
rs527478438	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100282750	GTCAAGGTATAGCTA[A/T]AACACATCTTTGCAG	25897
rs527527999	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283531	GATTTTTAGAAATAC[C/T]GTCCTTCAAACAAGT	25897
rs527598535	snp	C/T	1.65504e-05	0.00287662	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274976	CCAGACTCTTGACTA[C/T]AACTAATGGATGAAG	25897
rs527617123	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328593	TCTCTTGCCTCAGCT[C/G]CCTGTGTAGCTGGGA	25897
rs527619122	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320616	GACTATATCAGGGTG[A/G]TGAATGCCCATACAT	25897
rs527708914	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320978	GCTAAAAAATACTAA[C/T]GATCATCTGAGCCTT	25897
rs527720559	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267556	TAAATTTTTTTGAGA[A/G]ATGGGGTCTCACTAT	25897
rs527727281	snp	C/T	1.64925e-05	0.00287158	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258630	TTGTTTCTTTTAGTG[C/T]ATCGCCAAAATATAA	25897
rs527742215	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314952	TGCTGCGAGACACCA[A/G]TATGGTAAAGTATCG	25897
rs527762332	snp	C/T	0.00021518	0.0103703	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259206	TGAATTTGGATGGCT[C/T]TGACTCAATATCTAC	25897
rs527830747	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307756	AAACATACTGCTTTA[C/G]GACTTCACTTACATT	25897
rs527852369	snp	C/T	2.23586e-05	0.00334347	intron-variant	RNF19A	GRCh38.p7	8:100259827	ATTTAAAAAATACTT[C/T]CAATTTTTTAACAGT	25897
rs527866068	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100300377	AAATCAGCTGGGCAT[A/G]GTATGGTGGCTCATG	25897
rs527877694	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100330215	TTTTCTCTCTCCAAA[A/G]CCTCTTTCTAATTTT	25897
rs527916485	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100327449	TAGAGATGGGGTTTC[A/C]CCATGTTGGCTAGGC	25897
rs527951049	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100292497	TATTTGACTATATGG[A/C]AATTTTCCAATGTAG	25897
rs528071023	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100285260	TTTAATTTTTTCCTT[G/T]TATTTATATAACCTA	25897
rs528081435	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329173	TGCTGGCACAAAGCA[A/G]AAGTGGGTGCAAAGG	25897
rs528123631	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286007	CTAAAATTTGCTATC[C/T]TACTTGAAATCTACT	25897
rs528204968	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277229	CTGAGATTGCAATTA[A/C]GTTTTAAGATACTCT	25897
rs528205236	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100322977	TAATAACTTAAAAGT[C/T]TGAAATATTGTGAGA	25897
rs528209832	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269022	GCACTATATTAAAAC[A/T]ATGACTATTTTTAAA	25897
rs528286649	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289845	ACATACTTAACAATG[C/T]TCACAATAGCATTAG	25897
rs528289748	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323643	GTGTTAGAGGAAGAC[A/G]TATTTAAATAGTAAT	25897
rs528295434	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316326	AGAGCGAAAGAACGA[A/G]GCTTCCACAGTGTGG	25897
rs528325210	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100318364	CTCTTGGCTTAAATT[A/C]TCTGTTCCCATTTCT	25897
rs528337543	snp	G/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100260873	GTCCCAGTTCACACA[G/T]TCCTGGATGTCCTGA	25897
rs528345535	snp	A/G	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100316945	GCTAAGGGTCGGTGA[A/G]AAATCGAGCGCAGCG	25897
rs528431787	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310297	GCAGGAGCCGCCCCG[C/T]TGCACCCGGGTGGCC	25897
rs528457809	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311485	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	25897
rs528481039	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100303029	CTGATCATCATAGCA[C/T]ATGATATAAAACAAC	25897
rs528565426	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100306117	CAAATCATAAGGACT[A/G]TTTTTATCCTCAGGG	25897
rs528599896	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100334044	TTTGTGCCTACACCA[C/T]GCCTTTTCTTGATTT	25897
rs528645163	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100331074	CTACCCTTTAGGTTA[A/G]AATCCTAATCTCCTA	25897
rs528701887	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100276982	CACCGAGACAAACAG[G/T]GAGAAAGGTACATAC	25897
rs528719912	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279334	ACTAATCCTGCATTA[C/G]CACGTCAAACATTTA	25897
rs528723589	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286237	TTGAAAATTTAGCCC[C/T]GCATACGTCCCAGAG	25897
rs528760371	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100313701	TGTGGATCAGATTAA[A/G]GCAGAGCAAGAGTGG	25897
rs528762386	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100285343	CCCCCTCAAATAACT[A/G]ATTTTCGTAATTCTA	25897
rs528773940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100332695	TTGGTCTTTGCAAAT[C/T]TGTTAAAATGTTATC	25897
rs528774594	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100271859	CAAAAATCCTAAATG[A/G]AATTGTTTATGGTTA	25897
rs528803776	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100279709	TTTTTGTATCTTTAG[C/T]AGACACGGGGTTTTG	25897
rs528804901	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279769	AGACCTCAAGTGATC[C/T]GCCCACCTCAGCCTC	25897
rs528816253	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100325942	GTCCATGTCTGAACA[C/T]TCACAGAATTCAGGG	25897
rs528822820	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317781	GCAGGTGATGAGCAA[C/T]GACTTAGAGTGACCA	25897
rs528847256	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100326549	GAGGGAAACTGAGGT[A/G]ACCCCTCCCCCTTTC	25897
rs528896334	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263437	TTCTGGAGTGGTAGG[A/G]ACAAAAATCTGATTG	25897
rs529063287	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305192	CCTGCCTCAGCTCCC[C/T]ATACTGCTGGGATTA	25897
rs529066318	in-del	-/A	0.00119737	0.0244387	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337773	CTTTATTCAGCACTT[-/A]AAAGTCCTACTAACA	25897
rs529118611	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100274629	GCCTTAAGTGGTCGG[C/T]CCGCCTCAGCCTCCC	25897
rs529125965	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297113	TTACCACTGAAAAAA[A/T]TTTAAAGTTGATTAT	25897
rs529162092	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289446	GCACAGTGCCCAGAC[C/T]ATGTAAAGAATGCTT	25897
rs529254398	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326248	TGTTCTTTCTTCTGA[A/C]CTTCAGAAAAATGCT	25897
rs529307065	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282312	TATACAGATTGAGCA[G/T]CCCTAGTCAAAAAAT	25897
rs529314074	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100273223	TTTTTTTAAAACAAT[C/T]GCCTTGAGACTATTT	25897
rs529334574	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100261455	GTAGGGTTATATATA[A/G]TCATCATGCTTTATG	25897
rs529359387	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326725	TCTTCCAAGACCTTA[A/C]TCCTTATGGGCCTTA	25897
rs529381884	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274110	TTTTAAAGATGAGAC[A/G]AGTAACTTGCTCAGG	25897
rs529459346	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100265456	ACAGGTGTTAATAAG[C/T]AGAATTTGATATCAT	25897
rs529499068	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314097	ATGTCGCTCAGGTGG[C/G]TCTTGAACTCCTGGG	25897
rs529551927	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257457	TAAACAAAAGCAAAA[G/T]AAAATAATGCTAATC	25897
rs529598490	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306748	ATTATCCCTTAGTCT[C/T]TAGCTGTGCAGGTAC	25897
rs529776850	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291429	CCAGTTTTTTAACTG[C/T]GGAAAGACAAGAACC	25897
rs529815540	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283788	TAGCATTTCTGGAAA[A/C]GAACCTTTCAAGTGT	25897
rs529850390	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328661	ATTTTCAGTAGAGAC[A/G]GGGTTTCACCATGTT	25897
rs529884492	snp	A/C	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100275973	AAAAATAAAAAAAAA[A/C]TGTTTTTTTTTCCTT	25897
rs529912909	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100267845	ATGCCTGGCTAATTT[G/T]TTCTGTATTTTTAGT	25897
rs529968579	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100267642	CCCAAAGTGCTACGA[A/T]GACAGGAGTAAGCCA	25897
rs529992879	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329006	TTTATCAGTTTGGCT[A/G]CATGGTGATGACTCT	25897
rs530046068	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100321855	CATAATATTTTGAAA[G/T]ACATCTTTTTTCTGA	25897
rs530135006	snp	A/G	0.00636936	0.0560724	intron-variant	RNF19A	GRCh38.p7	8:100315620	GTTTCTTTCCCAGCA[A/G]GGTCATGGAAATTTT	25897
rs530174161	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301326	ATCTTACTGCCTAGA[C/T]TAGGCCTTCATTAAT	25897
rs530183628	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100317130	TGGCCCGCAAGCGCC[A/G]CACGCAGCCCAGCCC	25897
rs530208976	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100293135	GGCAATAATGCTCAC[A/G]GCTGCTCGCCTCCTG	25897
rs530260372	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100332962	GTCTATGGGTTCTCT[A/T]TTTGCTTTGTCTTAT	25897
rs530295631	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293515	TCTTTTTTTCCTTTG[C/T]TTGCATTCAACATTG	25897
rs530309646	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100278851	CAGAACATCAACCTC[A/G]CCGTTTAAAAATTTC	25897
rs530388944	snp	C/T	0.00318978	0.0398085	intron-variant	RNF19A	GRCh38.p7	8:100329985	GAGCTTAGATGGTCA[C/T]GTAAGGGATCCTAAT	25897
rs530440781	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100330720	TTTAGCTCTCCATCT[C/T]TTGAAGCCAAAGTAG	25897
rs530632035	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310372	CTCGAGCGCGCCGGG[C/T]AGTGGGGCCGGTGTC	25897
rs530736693	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100319822	GGCGTGAGCCACCGC[A/G]TCCAGGCTTTTTTTT	25897
rs530815079	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316244	GCAGCAGACCTTCGC[A/G]GTGAGTGTTACAGCT	25897
rs530874064	snp	G/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100295938	ATTTAAATGTTATTT[G/T]TAAGTTATGCCATTC	25897
rs530903539	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100278610	TTAGGAAGAATATAT[C/T]GTTTCTAAGCAAATA	25897
rs530908884	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100331900	CTCAAGAATATATCT[C/T]GGAGAATTACTATTA	25897
rs531028325	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288825	CAGCACTTTGGGAGG[C/T]CAGGATGGGCGGATC	25897
rs531098321	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100326028	ATGCTATCTGCTATC[C/T]GGGTGTTTTATGCTC	25897
rs531115045	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289116	TGATTTCTGACAAAG[A/G]TGATGTTGCTGAGAA	25897
rs531133337	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100273022	AGATGCCCATCACCA[C/T]GCCCGGCTAATTTTT	25897
rs531137549	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319096	GAATATATTTTACAA[C/T]TAGTTCATTTTGGAG	25897
rs531220632	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318580	TATGAAATATAACTG[C/T]AAGCAATGAGTAGCA	25897
rs531258667	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263705	GATATTTTTGTATTA[C/T]TGGTCATCCGTATTT	25897
rs531259905	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311928	AAGGACTTTCTATTC[C/T]TCACTAGGCCAAATA	25897
rs531274716	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100313418	GGAGGTGGGGAAGAC[A/G]GAGGAACAGCAGACG	25897
rs531347871	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100312601	TGTCTCAAGAAAGAA[C/T]GAAAGAAGGGAAGGA	25897
rs531356659	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100294817	CACGATCTCCACAAT[A/G]TAACTGCTTACTAGA	25897
rs531370554	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100301186	TATTGGCTACCATAT[C/T]GGACTGAACAGGTCT	25897
rs531383695	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289495	ATAGACAATCCAATA[A/G]AAAAACGGGCAGGGG	25897
rs531453741	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100327290	AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGGGTG	25897
rs531475651	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297249	GATGTACAATCTAAA[C/T]ACCTTTCAATTACTT	25897
rs531476308	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100305600	CACATTGTATTTCTA[C/T]TGGACAACACTGCTG	25897
rs531507677	snp	A/G	0.00358779	0.0422022	intron-variant	RNF19A	GRCh38.p7	8:100282641	TTCTAAGTCCCATGT[A/G]CTTGTTTTCTCTGGA	25897
rs531673551	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100334979	ATAAGCTCAGATCTC[A/C]CCAAACAATACCCTG	25897
rs531692744	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100313195	ACAGGCACTGAGACT[A/G]TAGCAATGAAAAAGC	25897
rs531765085	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100265721	GAAGGCTGTAAAGTA[C/T]GATGAGTGTTGTGGA	25897
rs531769596	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258487	ACCTGAAACTTAAGT[A/G]GTCACATGTAGTTCA	25897
rs531772316	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306810	CATCTTCTATCTACT[A/G]ACAGAGAACTGGCAT	25897
rs531801966	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314873	CTTAATGCCTGACAC[A/C]TAGTGAGAGAAAGAG	25897
rs531838726	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100307711	CCCAATAAAATAGAG[A/G]TGACCCAAGTGTCTT	25897
rs531849697	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100265911	GACCTTCCCAAGGTA[C/T]CTTTCATTATCCTTC	25897
rs531858065	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307120	TAATTTTTATCTTGG[C/T]AAAGAATGTTAAAAG	25897
rs531980694	snp	A/C/G	0.000131847	0.00811833	missense, stop-gained, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259146	CGCCAGCATGACTTC[A/C/G]GGTGGCACTGCCATC	25897
rs531992374	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292414	ATAGTTCTATTTAAT[A/G]AAGAGGCTTGCTATC	25897
rs532003475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100299383	CCAAGTATTAGTATA[C/T]TCTTCTTAGTAAATT	25897
rs532111684	snp	C/T	0	0	intron-variant	RNF19A	GRCh38.p7	8:100329097	TACCCTTTAATTTGA[C/T]ATAGGAGAGGGAGAG	25897
rs532213760	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284444	TACACAAAAGTAATC[C/T]CTGTGACTTTTTTTC	25897
rs532238686	snp	A/G	0.000100825	0.00709946	intron-variant	RNF19A	GRCh38.p7	8:100268963	CTAACGGAAAAAATT[A/G]TAATGTAAATAACTG	25897
rs532250380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100285072	TCTACTGTTAATGAA[C/T]ATTTTTTTGTTGTTG	25897
rs532252309	snp	G/T	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100275976	AATAAAAAAAAACTG[G/T]TTTTTTTTCCTTCGG	25897
rs532326896	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100260082	TAATTCAGTTAAGAA[C/T]CCTAGTAACCAGAAG	25897
rs532400582	snp	C/T	0.00795532	0.062565	intron-variant	RNF19A	GRCh38.p7	8:100297734	TGAGTGAGAAATAAA[C/T]TGTTATTGTGTTCCA	25897
rs532419796	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100331358	AAACAGATATAGGCC[A/T]GGTATGGTGGCTCAT	25897
rs532458365	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269722	TTCCAAATGACTAGC[A/G]TAATAACTTGGTTTC	25897
rs532483653	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316307	GTAGCAAGATTTACT[A/G]CAAAGAGCGAAAGAA	25897
rs532494529	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100308715	AATGTGGAATGTAAA[A/G]ATCACAATTTAAGAC	25897
rs532535232	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309437	GGAATGCGTTCCGCC[C/T]CCGCCGCCTCCCCGC	25897
rs532593315	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285218	TACACAATGTGGCAG[C/T]AGGTTAATCATTCAC	25897
rs532622386	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302238	AGGTATTAAGGATGG[A/T]AGCACAGAGAACAGT	25897
rs532660657	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100316375	TGCCACTGCTGTCCC[G/T]GGCAGCCTGCTTTTA	25897
rs532674208	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100274576	TTTTAGTAGAGATGG[G/T]GTTTCACCACGTAGC	25897
rs532722566	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100271091	CAAGTTTTATGGTCA[A/G]ACTTTACCTGTGCTT	25897
rs532735698	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294648	CAGCTGCCCTACACT[A/C]CATAGACTTTTCTTT	25897
rs532758568	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279298	AGGAGCAAACTAATA[A/G]CTGGTAGTGTAGGGG	25897
rs532774914	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100282703	AAATTTGTAAAAGGT[A/C]TACAACAGCATTTCC	25897
rs532813516	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100317052	CGGGACCAGCAGCGC[C/T]GCCCGGCTACTCTGA	25897
rs532851718	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330911	AAAAGTGCAGACTGG[C/T]TCCAAGGCTCTGAGC	25897
rs532863479	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307206	ACTTATTAATGACAT[C/T]AGAAAAACGAATAAC	25897
rs532911301	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311025	CTGAGAAACGAATGT[A/G]ATAGAGGCTGGACAG	25897
rs532943199	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303836	CCAGCTACTGGCAGG[A/C]TGAGGAATGAGAATC	25897
rs532968836	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311828	ATAAAGAAGCTGTGC[A/G]GAATGAAAATGGTCT	25897
rs533015940	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100266542	TGGAAATAGGGTCTC[C/T]CTGTGTCGCTCAGAC	25897
rs533028447	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304505	CCACCCCCACTTACG[C/T]ACTCACATTACTTAC	25897
rs533092214	in-del	-/GTTTTGTTTT	0.00281011	0.0373786	intron-variant	RNF19A	GRCh38.p7	8:100279365	ATATTTGATTGCCAG[-/GTTTTGTTTT]GTTTTGTTTTGTTTT	25897
rs533130691	in-del	-/GA	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100269338	CTCTGTAGCCTAAAC[-/GA]GATAAAATTTATGTA	25897
rs533149506	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100270998	TAAGAAAAGATATTT[A/G]TAGTGCTAACCACTG	25897
rs533206773	in-del	-/CT	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289674	GTGGAAGAATAGGAA[-/CT]CTCTTACACTACTCG	25897
rs533248647	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100333686	TAGCTGGGCATGGTG[G/T]TGTCTCCTGTAGTCC	25897
rs533284661	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326131	CACCCTTGACCTCAT[G/T]TCCAGCCTGGCTTTC	25897
rs533286143	snp	A/C	0.00318978	0.0398085	intron-variant	RNF19A	GRCh38.p7	8:100280775	TGTAATATATCAAGG[A/C]ATTAAATGTACCTGG	25897
rs533398490	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280043	TCTCTATACTCCCTA[A/T]GATTACTTATAATCA	25897
rs533417821	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319821	AGGCGTGAGCCACCG[C/T]GTCCAGGCTTTTTTT	25897
rs533492464	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100287068	GTAGGTACCTTTCAA[A/G]AGGGCCATTTATCTC	25897
rs533593204	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100319263	TATATGGTGATTCCT[A/G]CTCTTTTCCAGCAAG	25897
rs533632041	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100312666	CAGTGGCTCACGCCT[A/G]TAATCCCGGCACTTT	25897
rs533661172	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100281231	GGCTGAAACAGCAGT[C/T]TCTCCAGAAGTATCT	25897
rs533692198	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100331909	ATATCTTGGAGAATT[A/C]CTATTAATATATCAG	25897
rs533694449	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302954	GAGACTGGAGGGTAT[C/T]AAAACACTTCCTCTG	25897
rs533719912	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305262	ATTTTGTGCGGAGAT[A/G]TAAAACTGAGAGAAG	25897
rs533721821	in-del	-/ATACCCTAAG	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304414	TACTATATACATCAT[-/ATACCCTAAG]ATAACAGGCTTTTCT	25897
rs533765346	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100264965	CTCACAAATAATTTG[C/T]TCCTTATTAATTTGC	25897
rs533765733	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100274423	AGCAAATCAATCAGC[A/C]AACAAGTATAAAAAA	25897
rs533779359	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100329115	AGGAGAGGGAGAGGG[A/G]TGGTGTAGCTTACAG	25897
rs533813909	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100333442	GCTTAAAGCTATTAA[C/T]GACAAGAGAAAATGC	25897
rs533852751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100265876	ACTTCCCTACACAGT[C/T]CATGCAGGCAGAGAT	25897
rs533858068	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100280494	TTTATGCTACTTCTC[A/G]GTATTTTTTAAATGG	25897
rs533896478	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257754	CAGTCGATCCCAAAG[C/G]CACCAAGAATCAATG	25897
rs533953774	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306078	TCTACCAAAGTCTCT[A/T]CAATTGGCAACCTGC	25897
rs533996413	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319599	TAATGGCACAATCTC[A/G]GCTCATTGCAACCTC	25897
rs534085376	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312901	CACTCCAGCCTGGGC[A/G]ATAGAGCGAGACTCT	25897
rs534117845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291613	TTACACATCATTAGA[A/G]AGGTATTCTGGAAAT	25897
rs534156857	in-del	-/TG			intron-variant	RNF19A	GRCh38.p7	8:100268419	CTTTGCCTGAGGGCA[-/TG]TGTTATTTAGCTATT	25897
rs534168025	in-del	-/C	0.0111196	0.0737302	intron-variant	RNF19A	GRCh38.p7	8:100324828	CTTCCTTCCTTCCTT[-/C]CTCCTTCTTCCTCCC	25897
rs534169727	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100335813	TCTGCCCACAGTCCC[C/T]GCGGAGGTGCGGGCC	25897
rs534200085	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283987	CAAAGGCTTCAGTAA[A/G]CTTCAATAGGTCAGG	25897
rs534263621	snp	A/G			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337848	AGATTATCTAGTCTA[A/G]TAAATAATTGCTATT	25897
rs534288346	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320802	ATTGTGGGTTCAGTT[C/T]CAGACCACCAAAATA	25897
rs534322011	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100321189	AGCATGCACTGCTGC[G/T]TGGCAGCATTTTACC	25897
rs534369377	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100319935	CTGCCTCCCGGGTTC[A/G]AGCAATTCTCCTCCC	25897
rs534391595	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100322349	ACAAAACAAACTCTT[C/T]CCTTATACCTCATGA	25897
rs534410625	snp	G/T	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100315370	CATCAAAGGCAAGAA[G/T]CTTGGCCTTATGTTT	25897
rs534432452	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100259588	CAACCATCACCACTA[A/C]CTAACTTCAGAACAT	25897
rs534446690	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100308186	ACATTAGTTGCCAAC[C/T]GTAATTTTTTCCTCA	25897
rs534486915	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336416	AGAAACCGAACGACA[C/T]TGACAAGCACAGAGG	25897
rs534552320	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100312519	TCTCCATAGCCTTAG[G/T]AGGTCAAGGCAGCAG	25897
rs534601349	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100276041	AGGAATACCTTTCTC[C/T]GAGTTAATATTTCTG	25897
rs534630819	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267884	GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTTGA	25897
rs534680924	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337507	ATCCACTTCAGCTTC[C/T]GTGTCTCTCAGAATA	25897
rs534687791	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283345	TCAAGGCAGCTTCTA[C/T]GCTTCTCCTCCTTGC	25897
rs534748282	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329540	CAATGGTCCCACTGA[A/C]CTCAGCAATGGTCAG	25897
rs534843241	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287436	TTTTCTTTTGAGTAA[C/T]AGCAAATTATTTTAT	25897
rs534866721	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100301454	TGTGGCATTAAAAGC[C/T]CTCCACAGTGCAACC	25897
rs534905098	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278303	GACTATCATTTCTAC[A/C/T]TAAGTAATATAAATA	25897
rs534914224	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100271267	GCCAGACCAGGACAA[C/T]TGATAATTACTAGAA	25897
rs534933981	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100285735	CCTCATGGGTTCAAG[A/T]TACCTTCCCGTCTTG	25897
rs534934267	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100315283	ATCTATGTATACTCA[C/T]TCTAATATAAGAGCC	25897
rs534998664	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100261837	CCATGATTTCAGAGA[A/G]GACATTATATAAGGT	25897
rs534999309	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310156	CCCACTTCTTCCTCC[C/T]GCCCCCGGCCGCCCC	25897
rs535075468	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100267329	GGGTTAAAATAAGTA[A/G]AAGTACATACAACAC	25897
rs535118982	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277581	CCTCCCAAGTACCAC[A/G]TACTCTTTAAACACA	25897
rs535121767	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311140	ACAAACCAAGGAGCC[A/G]TGGTCTTTCCGAATG	25897
rs535156001	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304025	GCAATGTCGCAATCT[C/T]GGCTCACTATAACCT	25897
rs535234360	snp	A/C	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100324154	TAATTTATTTTTTAC[A/C]GCGGAGGAAGCCCAA	25897
rs535328839	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288968	GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC	25897
rs535329524	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317095	CCAAGCCCACGCCCA[C/T]GCCCACCCGGAACTC	25897
rs535341954	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325263	ACATGTTTGATACTG[A/C]AGGCAGAGAACTTAA	25897
rs535481286	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100272732	TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT	25897
rs535546886	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319309	TAGGATGAAAGTTTT[C/T]TTCTTTTTTAACACA	25897
rs535560023	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100275819	AAATGTAGTGACTAT[A/C]GGTTAGTTTTAACTG	25897
rs535683522	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305380	CAGTTAGAAAAAGAC[C/T]ACAAAAAGACAAGTT	25897
rs535705045	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279587	AGATGGAGTCTCACT[C/T]TGTTGCCCAGGCTGG	25897
rs535752766	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272201	TTTAAAATTTAACTC[C/T]AAGTGCCTAAACCTC	25897
rs535846049	in-del	-/A	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100275963	CTCCTGCCAAAAAAT[-/A]AAAAAAAAACTGTTT	25897
rs535872500	in-del	-/AGACCTGA	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100301891	GGTGGCATTTAGCAG[-/AGACCTGA]AGGAGGTAAAGGAGG	25897
rs535888527	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263945	GTAAAAGGATGGCAA[A/T]GGAAATTCTGAGTTG	25897
rs535908046	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334706	CCACTCCTTTCAAGA[C/T]CCAGCCCCGCTGGCG	25897
rs535931734	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312181	TATCCCTGTGCTCTC[G/T]GTTCTATATCTCCCT	25897
rs535975578	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305011	CACAATCTCAGCTCA[C/T]TGCAACCTCTACCTC	25897
rs535975973	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274468	AAAGTATTAAATGTC[A/G]AACATTCTGTGTTAA	25897
rs536070028	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100296634	CCACAGCTTTCAACA[C/T]ATTCTCCAAGGAGTC	25897
rs536075898	in-del	-/AAAGT			intron-variant	RNF19A	GRCh38.p7	8:100302554	CCAGAGATTAGGAAA[-/AAAGT]AAAGCCTAGAGATGT	25897
rs536079375	snp	C/T	0.00517822	0.0506191	intron-variant	RNF19A	GRCh38.p7	8:100266949	TGATTATAAAATGTA[C/T]GTTGAATATAAAAAA	25897
rs536162866	snp	C/T	3.29973e-05	0.00406172	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258703	AATATGATTCAACTG[C/T]GAAACTTCTGAACAG	25897
rs536193398	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289834	TACATTAAAAGACAT[A/T]CTTAACAATGCTCAC	25897
rs536283493	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326510	CAGAGCCAGTCCCTG[C/T]CCTAACAGATCTTGC	25897
rs536301454	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291694	AGAGGAAAACCTACT[A/T]CATGGTCAAATAACA	25897
rs536390901	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292546	ACGTGCTCAAATTCA[C/T]ATATCTTTCTGACTT	25897
rs536412772	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100327865	CAGGGACTCAGAATA[C/T]GTGATCAAGAAGCAC	25897
rs536427621	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284533	CAAATTAATCACGGA[C/T]AATTATTTGTTAAAT	25897
rs536451811	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100313756	TATTCCAGGAATCCA[A/T]TAAAGATGTCATAGT	25897
rs536484846	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328858	GGTTATAGACTTGTG[C/G]AAAGGGTCTTCTATA	25897
rs536525336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100321529	TCAAAGTCATGCATG[A/G]GAGTTGGAGTCAACT	25897
rs536525528	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100308879	GAACATTCTGCAACA[C/T]TGTGGACAGTAAACA	25897
rs536605861	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100299732	CATTGCACTCCAGCC[C/T]GGGTGACAAGAGCAA	25897
rs536667697	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307832	TTATTTATTCATCCA[C/T]TTTCTTGAATGAAGT	25897
rs536695661	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100325475	ACCACACCTTGTCAC[C/T]TCTAGGTCCTCCCTT	25897
rs536705832	snp	A/C	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100300499	CTCTACAAAAACTAC[A/C]CAAATTAGCTGGGTG	25897
rs536738211	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100316470	GTGCTGATTGGTGCC[C/T]TTACAATCCCTGAGC	25897
rs536740606	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100309105	TGCAGAGTGGAACCC[A/G]GATAAGAAAAACTGA	25897
rs536962914	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100302517	AGGTGGAGATGTATA[A/T]CCAAACACCCGTTTG	25897
rs536989713	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294749	TTTGAGATACAGTAT[A/T]CTTGAATCTGTACAG	25897
rs537025531	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330412	GACCTGTAAGGGTTA[C/T]GATCTTTGCCTGGCA	25897
rs537094720	snp	A/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100315091	GAGGCAAGCAGATGA[A/T]TTGGGCCTAGGCAAC	25897
rs537167469	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100260957	TTGTTACCCACAGAG[G/T]TAAGATCTAGGCTTA	25897
rs537184719	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325068	CCTACCACCACAACC[A/G]GCTAATTTTTTGTAT	25897
rs537213197	in-del	-/TTT	0.00358779	0.0422022	intron-variant	RNF19A	GRCh38.p7	8:100285981	ATGACTCACAAAAAG[-/TTT]TTTTAAAACTAAAAT	25897
rs537268257	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302475	GTTCATTTTTAGACA[C/T]TTATACTTGAGATAT	25897
rs537319181	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100287405	CTGTTGAATGAATTC[C/T]CCAGCATGTAAAAAT	25897
rs537373554	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100290349	TCAAGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	25897
rs537421056	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287172	TCATCATAAACAAAC[C/T]TGATCATTTCATCTG	25897
rs537425327	snp	A/T	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100277797	AGACCCTATTTTTTT[A/T]AATCAAAGTTTTAAT	25897
rs537459127	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304644	CAGGCAATATTAAAT[A/G]GATGAGAGGTTTAAA	25897
rs537463818	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100331167	CAACATTCACAGCCT[G/T]ATCATCTTGGGTTTA	25897
rs537481252	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272305	TATAAATATTGTATT[A/G]TTTTATAAACACAAA	25897
rs537551595	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100324346	CAAGTTCAAGAGTTT[A/G]GATGACTAAAGTTGA	25897
rs537561796	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271412	ATACAACACGTGGTA[C/T]ACTAAATTAAGGAAA	25897
rs537578498	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317159	CCGGGTTCCCGCTCG[C/T]GCCTCTCCCTCCGCA	25897
rs537623472	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100325780	TTACACACACACACA[C/G]ACATTTATATCCATA	25897
rs537629825	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100280359	TGTAGTGTTTGTGTG[C/T]CTGTGAAGAGAGATG	25897
rs537715841	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100281047	TCTCTGACTCAAACA[A/G]CCCCCAGACCTTAGT	25897
rs537746865	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326282	TCAATTCTCTTTAAA[G/T]GCATACCACCTAACC	25897
rs537757142	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100273359	GTCACATCTTACTTT[C/G]CATCTATACCAAACC	25897
rs537778168	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304181	TGGCCAGGCTGGTCT[A/C]GAACTCCTAACCTCA	25897
rs537848734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100264846	TTACAATTTAACTTA[A/G]TTGAAAAAGATCTAT	25897
rs537864303	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100295714	AAGCCATCCTTTGAT[C/G]AGACTATAACTTAAA	25897
rs537871125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312836	GACTGAGGCATGAGT[C/T]GCTTGAACCTGGGAG	25897
rs537909683	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100313555	AAAGTAGGAGGCAGC[C/T]GGATGATTTAATACC	25897
rs538012303	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100333368	TAAGACAGCTGTTGT[C/T]TTATAAGTAAATCAC	25897
rs538114035	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272796	CTCAAGCAATCTGGC[C/T]GCTTTGGCCTCCCAA	25897
rs538124244	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100333668	AAAATTTTTTTAAAA[A/C]AATAGCTGGGCATGG	25897
rs538132227	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334796	CAGAGACTCCAAAGA[G/T]ACGGTCTTTAGATAA	25897
rs538142799	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318842	GCTGTTGGAAACGAA[A/G]AAAGGGAGAGGAAGA	25897
rs538149089	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263990	CCTCCCCACTACTTA[A/C]ACTGTTAATAAGCAC	25897
rs538255288	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100316753	TGGAGCTGCCTGCCA[A/G]TCCCGCACCGTGCGC	25897
rs538361057	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257493	TGGACCTTTTGTACT[G/T]GGTACAAGTTCTGCA	25897
rs538362105	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267042	GAAATAAAGGAAACA[A/G]AAGGAAACAGATCTG	25897
rs538395347	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100296376	TCCCCAAGTGCTGGG[-/A]TTACAGGCGTAAGCC	25897
rs538499700	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100326906	AGTGTTATCTTATAC[-/T]TCTTTTCCTTTTGAA	25897
rs538537904	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291474	GTGCTTCAGGATTCG[G/T]AAAACATGTTAAGTA	25897
rs538544902	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282995	TATGTTAGTAGCATA[C/G]AGTCAGGCTGGTTCA	25897
rs538615578	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305255	CAAAGTCATTTTGTG[C/T]GGAGATGTAAAACTG	25897
rs538618670	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283879	CCATTTTTATAAAAA[C/T]CAAATATTCAGAAAT	25897
rs538630932	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274601	CGTAGCCCAGGCCGT[C/T]CTCGAACTCCTGGCC	25897
rs538640426	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292730	GTTACTGAATAATGA[A/T]CTTTCCTCCATGCCC	25897
rs538705579	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275318	TATAAAAATGGGGGA[A/C]AATGAAGTTTACAAA	25897
rs538717281	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284694	TTTTACTTTTTAACA[A/G]TGAAGTCTCAATGAG	25897
rs538771341	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291411	CATACGGCCTTACTA[C/T]ATCCAGTTTTTTAAC	25897
rs538775786	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314554	CACAGTAAGGTACTA[C/G]CAGTACCACAAATCC	25897
rs538840239	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100276546	CACTTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG	25897
rs538851342	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100315232	GTTGTAGGGTGCAGT[A/G]AGCCAAGATCACACC	25897
rs538861115	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100259467	TTTATTGCTTATGCT[A/G]TTCTAGACACTATGC	25897
rs538875215	snp	A/G/T			intron-variant	RNF19A	GRCh38.p7	8:100284407	AACTAACAGAGCAGT[A/G/T]TAAGTCAAATATAAA	25897
rs538876755	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100277463	ACTACAGGCGCCCAC[C/T]ACCACGCCCAGCTAA	25897
rs538893015	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269490	CAGTTTTTTAATAGT[A/G]AACTAATGCAAAACA	25897
rs538893246	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307991	ACAGTATGGACAGTT[A/C]TTTATATTAAGTCTA	25897
rs538910426	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100309148	GTAGTATTACTTGCC[C/G]GGCGAGGGCTGGGAA	25897
rs538964389	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270230	AACATTTTTAAAACA[C/T]AGTAGTAAAACAATG	25897
rs539019014	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301382	ATCCTCTTTGTTAAA[A/G]TCTGCTTACAAATTT	25897
rs539051318	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258457	TATGATAATGAAACC[C/T]GGCTTTTGCTGGTAA	25897
rs539066417	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100310097	ACCAGCGCCGCAACT[A/G]CCACCTCCCCCTCCC	25897
rs539080848	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336752	TTGTTTTTTTTTTTT[C/T]TTCTTCTTTGGAATT	25897
rs539088193	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100290942	AGTGCCTCACACTGG[A/G]TAAATCCAACCAGAA	25897
rs539108930	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302525	ATGTATATCCAAACA[C/T]CCGTTTGACAAGCCC	25897
rs539109026	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310457	GTGGCTGGAGCTGCG[A/C]CCGGTTGAAGGGAGT	25897
rs539191824	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303275	AAGCATTCCTCGGCT[C/T]GCGGTTACATCACTC	25897
rs539206995	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329318	TCAAAAAATGCCACC[G/T]ACATAGTTACAAAAG	25897
rs539244131	snp	G/T	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100330048	GCTTATAGGAGAGGT[G/T]GGGGAAGTTGGATTA	25897
rs539329904	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100331353	CAGAAAAACAGATAT[A/T]GGCCAGGTATGGTGG	25897
rs539373582	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100261017	AGCAGCTGTAGCAAC[A/G]ATTTATAATATAAAA	25897
rs539601720	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263861	AATTACCCCCACCTC[C/T]TTCATCCATACACTC	25897
rs539602646	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294823	CTCCACAATATAACT[A/G]CTTACTAGACTGCTT	25897
rs539631319	in-del	-/C	0.00318978	0.0398085	intron-variant	RNF19A	GRCh38.p7	8:100277478	ACCACGCCCAGCTAA[-/C]TTTTTTTGCATTTTT	25897
rs539690060	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287318	GCAGAGACGATATAG[A/C]AATGAGTAAGATAGG	25897
rs539753729	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278729	ATTCATAGCACTACA[C/G/T]TAACTTTAAAGAACT	25897
rs539809030	in-del	-/CCTC			intron-variant	RNF19A	GRCh38.p7	8:100324838	TCCTTCCTCCTTCTT[-/CCTC]CCTCCCTCCCTCCTT	25897
rs539832869	snp	A/C	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100271495	AGAGTATGCTCAAGT[A/C]GTAGGTATCTCAACA	25897
rs539838656	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279514	AAGTAACTGAGATTA[C/T]AAGCGTGAGCCACCA	25897
rs539906544	snp	A/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100272384	AAAAAAACAACTAAT[A/T]ATTATACCAATTAAT	25897
rs539919754	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318106	GGATTTATAGGAGCC[A/G]TGAAACTTGTTGCTA	25897
rs539938019	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100262833	GAAGTGGCTGGATTA[C/T]GGCTAAATATTGAAG	25897
rs539956073	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311398	TAGTAAGTTAAGTAC[C/T]CATATATAATATCCT	25897
rs540029232	snp	A/G	0.000232087	0.0107698	intron-variant	RNF19A	GRCh38.p7	8:100264233	ATTACAAACAACAAC[A/G]ACAAAATAACTCACA	25897
rs540058453	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312459	TGGCATGGTGGCCCA[C/T]GTCTGCAGTCCCAGC	25897
rs540061095	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304404	ACAGTCATTGTACTA[C/T]ATACATCATATACCC	25897
rs540184886	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100296411	CGACCAGCCTCCGGG[A/C]ATTATTCTTACTGCC	25897
rs540190585	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100332578	CCAATTATCCTACAA[C/G]TGATCACATAAATCA	25897
rs540246998	snp	A/G	0	0	intron-variant	RNF19A	GRCh38.p7	8:100297585	TCATCCCTGAAAAAA[A/G]CCTTCAAGCTCTCTT	25897
rs540301782	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100318407	GATTGAATTTTTCTC[A/G]TGCTATATTTTATGT	25897
rs540310783	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291803	GTAATTTTGTGCTGA[C/T]GGTCAAAATACTAAA	25897
rs540311490	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325864	CATTTTCTTCCTTCT[C/G]TCCTCTTTTTAAAAT	25897
rs540319227	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290202	TCACTGCAGCCTCCA[C/T]CTTTTGGGTTCAAGC	25897
rs540326244	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263399	CACTGGTGACTCTGC[C/T]TCAGTGAATAGCAGA	25897
rs540382288	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326680	TCTTATTTCCTTCCC[A/G]TGAGCTCTTGAATTC	25897
rs540419948	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282054	TTGTTCTCAGGGCTA[C/G]ATGCCTGAGACTAGT	25897
rs540466909	snp	A/G	0.00358779	0.0422022	intron-variant	RNF19A	GRCh38.p7	8:100327326	GCATGATCTTGGCTC[A/G]CTGCAACCTCTACCT	25897
rs540467020	snp	A/T	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100319836	CGTCCAGGCTTTTTT[A/T]TTCTTTTTTTTTTTT	25897
rs540660729	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258107	TGTTACAGAGTATCA[C/T]ATACTGAGAGTAACC	25897
rs540671248	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306662	AAGTTTTAAACACCC[A/G]AAGTGATTTCACTGC	25897
rs540808709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283125	TTAATTATGTCCCAG[C/T]ATAATAAATGTTCTT	25897
rs540826691	in-del	-/C	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310301	AGCCGCCCCGCTGCA[-/C]CCCGGGTGGCCCCGA	25897
rs540842337	snp	C/T	0.00517822	0.0506191	intron-variant	RNF19A	GRCh38.p7	8:100294804	CTACTTATGCATCCA[C/T]GATCTCCACAATATA	25897
rs540891914	snp	C/T	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100274626	CTGGCCTTAAGTGGT[C/T]GGCCCGCCTCAGCCT	25897
rs540893718	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100265348	CCAGGGCTCTCATTT[A/T]TAGCTCAAAGTAAAT	25897
rs540895056	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	RNF19A	GRCh38.p7	8:100336141	GGTAGCGAAGAAATG[C/G]AGGGCATGGGTCCCA	25897
rs540919451	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284176	AATTTTGCTAGTAAT[A/G]GCATTAAAGATCTCA	25897
rs540928697	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100266352	TGACCTGAACAATGA[A/G]GTAAATAATCTCTTC	25897
rs540982000	in-del	-/ATG			intron-variant	RNF19A	GRCh38.p7	8:100284617	TGTTTCTATTATTTT[-/ATG]ATATTTTATATTTGA	25897
rs541015586	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275968	TGCCAAAAAATAAAA[A/G]AAAACTGTTTTTTTT	25897
rs541027218	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314752	TAAATCAAGCTCACA[C/T]TCCCTAGCTCCACAA	25897
rs541041765	in-del	-/TT	0.00358779	0.0422022	intron-variant	RNF19A	GRCh38.p7	8:100278493	AATCTTTGTGATGAC[-/TT]TGTAAAAGCCAAATT	25897
rs541049659	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258928	TACAGAAGGCATACT[A/G]TCACTGAGGGATGGA	25897
rs541099000	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100335437	AGAGATATCTACTCA[A/G]CAACTTCCTAGTTTC	25897
rs541108456	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100306341	TCTGTCATATTGAGA[A/G]TTTCATGTAACAAAA	25897
rs541114835	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100299082	ACAGACACATTTTGC[C/T]TACTGTGTCCCTTGG	25897
rs541138546	snp	A/T	2.01157e-05	0.00317134	intron-variant	RNF19A	GRCh38.p7	8:100259832	AAAAATACTTTCAAT[A/T]TTTTAACAGTTTTTT	25897
rs541138816	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269572	CCTAAATGATAAAAT[G/T]TATGTATGGGAAAAT	25897
rs541142101	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100315542	ATTGGAATGTGCTAC[C/T]TCTTGACTCTCCTCC	25897
rs541182970	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100277469	GGCGCCCACTACCAC[A/G]CCCAGCTAATTTTTT	25897
rs541232472	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100332689	AACATTTTGGTCTTT[A/G]CAAATTTGTTAAAAT	25897
rs541241263	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291898	GTATGGTACTTCTAA[A/G]ATAAGCATGCAATAA	25897
rs541314853	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301942	GAAATCTGGGGAAAG[A/G]GCATCCAAGGCACAG	25897
rs541332985	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336800	AGTTTTTCTGTTTCC[A/T]CCTTTGCTGCTAGGC	25897
rs541352709	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328618	CTGGGATTACAGGCA[A/C]GCGCCACCACACCCA	25897
rs541475216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286042	TTTCAAGAGTATAAC[C/T]TGCACATGTGCACCA	25897
rs541475571	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100321831	TGACTAGGTGAATTG[G/T]CAGTGAGACATAATA	25897
rs541514373	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100322655	TTTTGGCCTGCCTTC[C/T]TCATTAAGCTTAATC	25897
rs541574307	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323706	CTAATTGAAAGTTTG[C/T]GTGATATGAAAAGAT	25897
rs541611993	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100331509	GGGCATGGTGGCATG[C/T]ACCAGCAGTCCCAGC	25897
rs541636714	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278854	AACATCAACCTCGCC[A/G]TTTAAAAATTTCATG	25897
rs541662245	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100316972	AGCGCCGGTGGGCTG[A/G]CACTGCTGGGGGACC	25897
rs541791600	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100314082	AGACGAGGTTTTGCC[A/G]TGTCGCTCAGGTGGG	25897
rs541861976	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286981	TCCAATATTACATAA[A/C]CCCTAGAACTTGAGA	25897
rs541923022	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100330804	TCCCATGGCTTCTAA[A/G]GCCCAAGAAAACTTG	25897
rs541947771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278041	TTAGCGTGGCCAGTT[C/T]AAATTCTACTTCCAC	25897
rs541973886	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100291360	TAAATGAATGAATGA[A/T]GCTTTTCAGTTGCTA	25897
rs542063521	in-del	-/A			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288904	CTCTTTTAAAAATAC[-/A]AAAAAACTAGCCGGG	25897
rs542119877	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100261312	CATGTTGCCCAGGCT[A/G]GTCTCGAACTCCTGA	25897
rs542198690	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280574	ATTTATACAAATTCC[A/G]AAGAAAAACATGTTT	25897
rs542210676	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100325994	TATCCTATTACAAAT[C/G]TATGTGCTACAAAGC	25897
rs542229078	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100329377	AAAAAAAAAGACTTG[G/T]GATTTTAATGTTCAC	25897
rs542254684	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100302978	TCCTCTGATATTTCT[C/G]AGAATTAGAATTCTA	25897
rs542287694	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100264459	GCCTCCGAACTGTAC[C/T]TGGGGTGGAGTGGGG	25897
rs542371471	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280438	AAGGAGAGTTTAGTT[C/T]ACGGCATGTTATATT	25897
rs542413998	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF19A	GRCh38.p7	8:100257005	GAATACTACCACATG[A/G]CCAATGAATATTCTC	25897
rs542459194	snp	C/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100277767	TTATTCATCGCAGTC[C/G]CAGATAAAGAAAAAA	25897
rs542493459	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289167	AAAAAAGAAAAATAC[C/T]ATGTCTACTGGTTAT	25897
rs542494665	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325532	GTTTCAACTTTATAT[G/T]TACCCAGGAATTTGG	25897
rs542540128	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100303041	GCACATGATATAAAA[C/G]AACGATAATTAGAGA	25897
rs542544845	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290252	GGATTACAGGCATGC[A/G]CCACCATGCTGGCTA	25897
rs542548574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297670	AGGACAGAGGAGTCA[C/T]AAGATGGAAAGAATC	25897
rs542555872	snp	A/T	0.00953873	0.0683987	intron-variant	RNF19A	GRCh38.p7	8:100272553	CTTTTTTTTTTTTTT[A/T]AATTAATAGGGTCTT	25897
rs542627440	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100290923	GGCTCTCCGATATCC[C/T]GCCAGTGCCTCACAC	25897
rs542629360	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282519	TAACTCTTATAATAT[A/G]TTTATGTATGTGTGT	25897
rs542673265	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100308417	AGGAAAGAACATTTG[-/A]AAATACGATCATCGC	25897
rs542680817	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100273795	TTATCATCATTATTA[C/T]TTTTTGAGATGGAGT	25897
rs542703935	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334968	CTAGGGTTAAAATAA[A/G]CTCAGATCTCCCCAA	25897
rs542722662	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319673	TAGCTGGGATTACAG[A/G]CACACACCACCATGC	25897
rs542722793	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100312546	GCAGTGAGCCCTGGT[C/T]ACACCACTGGCCTCC	25897
rs542753932	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100284060	ACATAGGTGCATTAA[A/G]TATTTGAATGATTAT	25897
rs542772930	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305197	CTCAGCTCCCCATAC[C/T]GCTGGGATTACAGGA	25897
rs542784849	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320406	TACATGTATCTTCTT[G/T]CTCATGCAGGAGAGT	25897
rs542799904	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100274726	GACTATCTTTGGCTA[C/T]CAGTTATATAAATCA	25897
rs542823563	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314116	TGAACTCCTGGGCTT[A/G]AGTAATCTGCCCAGC	25897
rs542825918	in-del	-/TTAAA	0.00398564	0.0444627	intron-variant	RNF19A	GRCh38.p7	8:100281413	ATTTTCTTAATTTAC[-/TTAAA]TTAAGTCATTTATAA	25897
rs542978942	snp	A/G	0.00398564	0.0444627	intron-variant	RNF19A	GRCh38.p7	8:100315402	TTTCACTGGGGGGGA[A/G]AAATGCAACCAGGAA	25897
rs542985903	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307656	TTACCCATATTTAAT[C/T]CTAAACAACCCCATA	25897
rs543058529	snp	A/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257299	CACCATAATGGTAAT[A/T]CTTAAAAGAAATACA	25897
rs543071845	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100300125	AAGAGGCACAATAAG[C/G]AAAATGTGTCTGTTT	25897
rs543104432	in-del	-/A	0.10752	0.205425	intron-variant	RNF19A	GRCh38.p7	8:100333081	CATTTCTAGTATGGA[-/A]AAAAAAAAAGAACAA	25897
rs543125157	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100294917	AACGAATGACTAAAT[A/G]TGTTAAACTTTTTGC	25897
rs543190724	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275592	CAAATTGCATTTAGC[A/C]TAATCTCAATTTTAT	25897
rs543240502	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337797	ACTAACAATAAAATT[G/T]TTTGTTGGTGATATT	25897
rs543277056	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100267293	TTAACACACAGAGAC[C/T]GAAATATCGAGGTTG	25897
rs543308985	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276320	TTACACCGAGTGAAA[A/G]AAGTCAATCTCAAAA	25897
rs543337533	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100297364	CTTTTGTTCAGAAAG[C/G]ACCTCTCTGTATCAT	25897
rs543351210	snp	C/G/T	9.88621e-05	0.0070301	synonymous-codon, missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259114	AGATTTACCTTCAGG[C/G/T]AAGCCACTGGATGAA	25897
rs543440872	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100259620	TTCATGATCCCAAAA[A/G]GGGATCTTGCATCCA	25897
rs543489991	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100312677	GCCTGTAATCCCGGC[A/C]CTTTGGGAGGCTTAG	25897
rs543523182	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270604	ATTTTACTTCACACA[A/C]AAGAGAGATGGACCT	25897
rs543528176	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100285078	GTTAATGAACATTTT[G/T]TTGTTGTTGTTATTG	25897
rs543572612	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292924	CTTGTGCAGCGGTGC[C/G]CAAACTTTTTGGTAC	25897
rs543660021	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293235	CCACTTTTCATCTGG[C/T]GTCATGTATCTTCAG	25897
rs543717101	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303451	TTAACTTAATTACAT[C/T]TGCAAAACCCCTTTT	25897
rs543744059	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277035	ACTGCATGTGAATCT[A/G]CCATTACCTCTATAA	25897
rs543747921	snp	A/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100325706	TTATCAACCTCAATA[A/T]TGCAGAAAATATCTG	25897
rs543749611	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287076	CTTTCAAAAGGGCCA[A/T]TTATCTCATATGAGA	25897
rs543782419	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100269671	AACAAAAACAAAAAA[A/G]GGAAATATCCATTTC	25897
rs543801860	in-del	-/T	0.00255689	0.0356638	intron-variant	RNF19A	GRCh38.p7	8:100277790	GAAAAAAGACCCTAT[-/T]TTTTTTTAATCAAAG	25897
rs543807991	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100295111	TGAACAGATACTTCA[G/T]ATGATATCTTCTCCA	25897
rs543821211	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100268105	ACCAAAGAAAATTTC[C/T]TTTTTTTTTCTTTTA	25897
rs543832677	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100316271	AGCTCATAAAAGCAG[C/T]GTGGACCCAAAGGGT	25897
rs543969234	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310241	GCTGCGGGCGGCTCT[A/G]GACGCGGCTGTTCCC	25897
rs544052193	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100294552	CTCCCTCCTTTCTGC[A/G]ATTTATCCTATTTCT	25897
rs544100081	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311716	GAGCGAGACTCCGTC[C/T]CAAAAAAAAAAAAAA	25897
rs544137568	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312409	AGGAGTTCAAGACCA[A/G]CCTGAGCAAGATGGC	25897
rs544148909	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263091	GTTACACATGCAAGT[C/T]TGAAGTTCAGGGGAG	25897
rs544219140	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305081	GCTGGCATGACAGGT[A/G]CCTGCCACCAAGCCC	25897
rs544254894	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289132	TGATGTTGCTGAGAA[C/T]TGAGAATAAATGGCC	25897
rs544270352	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100331580	ATGTCAAAGCTGCAG[A/T]GAGTCATGACTGTGC	25897
rs544277912	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100324716	AAATTCAAAATAAAT[A/G]AACAGAACTTCATGA	25897
rs544360443	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100263152	GATTAGGGGAAAAGT[A/G]TAGATACATAAGAAT	25897
rs544370077	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100297280	CAATGTGTCCTTAGA[C/T]GCGTGAGCACATAAT	25897
rs544562175	snp	C/T	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100326580	CTGCTTTACTGATAC[C/T]ATTCAATAAAGGGGA	25897
rs544568778	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100319299	AAATTTTTCTTAGGA[G/T]GAAAGTTTTTTTCTT	25897
rs544647895	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100319794	CTCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGC	25897
rs544759631	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100259612	AGAACATTTTCATGA[A/T]CCCAAAAAGGGATCT	25897
rs544773606	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289981	GAATAAAATACTGCT[A/G]CACACAAGACAGGAC	25897
rs544802328	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280726	TCACATTCATATGTA[C/T]TCAATCCTAACCATA	25897
rs544888231	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100273064	TAGAGAAGGAGTCTC[A/G]CCACATTGCCTAGGC	25897
rs544890489	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100281963	TCTCCTGGTTCCCTT[C/T]TTTAGGATTTGCAAC	25897
rs544925477	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100273869	CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG	25897
rs544935876	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291147	ATCCTAGGTAAGATA[C/T]ATTCCTGAATCAGTG	25897
rs544949275	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283320	GCAGAGGGTAATCAG[A/G]TATTTTTATTCAAGG	25897
rs544987217	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100280683	TTTCTCACACTAACA[C/G]TTATTGAGTGCTTCC	25897
rs544995958	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320257	AAATGATTTTATACT[A/G]AATGTATCATTTTAT	25897
rs545025965	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303555	AAAATATGGTTCTGG[A/G]AATTTTTGCTAAGGA	25897
rs545065464	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275872	AATTTATAAATTTTG[C/T]GATAATTTTGTATGT	25897
rs545087557	in-del	-/AT	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100280584	ATTCCGAAGAAAAAC[-/AT]GTTTACTTTAATAAT	25897
rs545102154	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100329782	AAGAAGTAGCTTCAT[C/G]GTTTGTTAATCCAGA	25897
rs545105224	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258077	AAATGAAATTTATGC[C/T]GATATAAATAGAAAT	25897
rs545118637	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100313861	TCAGTCATACTTGCA[C/T]GGAATGGAATAAAAG	25897
rs545124409	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100305601	ACATTGTATTTCTAT[A/T]GGACAACACTGCTGA	25897
rs545161438	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306434	TAAAATACTAGATAA[C/T]ATCAATAGGATAAGA	25897
rs545200018	in-del	-/GTTTT	0.0131103	0.0798953	intron-variant	RNF19A	GRCh38.p7	8:100279370	TGATTGCCAGGTTTT[-/GTTTT]GTTTTGTTTTGTTTT	25897
rs545264223	snp	G/T	3.29826e-05	0.00406082	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259173	CATCATCCACACTAC[G/T]GCTTCCACTGTTGTG	25897
rs545295479	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100308460	AGAGAAGTATTTACA[C/T]TTTAACTCAATTCAG	25897
rs545330835	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100309209	CCCGGAAGACCCCCG[C/T]TAACACATACTTCAC	25897
rs545332520	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100291736	TGTTATTCAGCTAAA[A/G]TTAGGTTTCTTCTGT	25897
rs545341496	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335169	CTAATATGTTAGTAC[A/C/G]TAGCTCCCCTATTTA	25897
rs545395260	in-del	-/AAAC	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100329445	AAACAAAACAAAACA[-/AAAC]AAACAAACAAACAAA	25897
rs545500760	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337974	CATTGTAAAACTAGT[C/T]TTGTGGTTTGGTTTG	25897
rs545554961	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100321666	ATCAGAGGAATCACT[A/C]TCTATGGAAGCTATA	25897
rs545591702	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315450	GCTTTAGTCTCCACC[A/G]TCATTTCACCTGGCT	25897
rs545637333	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330671	TGAGTCTCTGGACTT[C/T]CCAGTTACCCAAGGC	25897
rs545665590	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286813	ATTCCTGAATAGTAT[A/G]TGACTACTGTTTCCC	25897
rs545722829	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100322953	TACAGATCACCATAA[C/G]AGATATAATAATAAC	25897
rs545756094	snp	C/G			utr-variant-5-prime	RNF19A	GRCh38.p7	8:100336154	TGCAGGGCATGGGTC[C/G]CACACTCAAATGCCC	25897
rs545886327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317335	TGAGGACTGCCAGCA[C/T]GCTGTCACCTCTCAT	25897
rs545896216	in-del	-/TAG			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288369	ATGTTTCTTAACCAT[-/TAG]TAGTAGTTGTTTTTT	25897
rs545978208	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310788	TATTTTGCAGTCAAG[G/T]AATCAGAATTCCTAT	25897
rs546033488	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100286187	AGTTATTTAAAGCTA[C/T]TATTCATTATTCCTA	25897
rs546058962	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323493	TTTCTGCCATCCATT[C/T]TTAGAATTGTCACAT	25897
rs546065704	snp	G/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311350	CAGCGACTTTACATA[G/T]GGGATGCTTTAAGCC	25897
rs546084549	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269791	AAGTATCTTATAAAA[C/T]CCAAATTTAAGACAA	25897
rs546092638	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100266162	TGCCACATTCTCTAC[G/T]TTTTATTGTTAAGTG	25897
rs546092689	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277903	TTTTTCTCTACCTAC[A/C]TTTTATTGAAGGAAG	25897
rs546127591	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100271494	CAGAGTATGCTCAAG[A/T]AGTAGGTATCTCAAC	25897
rs546137834	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279300	GAGCAAACTAATAGC[C/T]GGTAGTGTAGGGGAA	25897
rs546145179	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316864	GCCGCACAGCAACTC[A/G]TGGAGTGGGTGGGAG	25897
rs546156497	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100295893	CACTGAAGTTCATTA[C/T]AATAAAGTTTGCTAT	25897
rs546174195	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100298781	TATTACAAAAAGTAA[G/T]CTGCTGCAGAAAGGA	25897
rs546229175	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310260	GCGGCTGTTCCCTTG[A/C]GCACGTTCGTTCCGC	25897
rs546237589	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100333427	AGCTACAAAAACAAA[A/G]CTTAAAGCTATTAAT	25897
rs546287444	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100286611	CAAGAAACTTTTAAA[C/T]AGTGGATTTGATTCA	25897
rs546321990	snp	A/C	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100317698	CTGGTTAGACAAACT[A/C]CATGTTTGACAGGAT	25897
rs546353385	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303859	TGAGAATCGTTTCAG[C/T]CTGGGAGGCGGAGGG	25897
rs546353961	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303603	AAATTATGCAAAAAT[A/C]TAAAGGATATTTAAC	25897
rs546358643	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311071	TCTGTTACTTAACTA[A/C]ATATATCACTCTCCC	25897
rs546392215	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304531	CTTACCAGTTCCCAC[C/G]TCCACTTTCCAAATG	25897
rs546478791	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100295766	ATTTCTACCCAAGCT[A/G]ATTTTGGCCCAAAGT	25897
rs546480316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100296251	CTGTGACTACAGGCA[C/T]GTGCCACCATGCCTG	25897
rs546520180	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100271129	TAATTCAGGTTTCCT[C/T]AGCACTTCTTCTAGG	25897
rs546551438	snp	C/T	0.00011556	0.00760044	intron-variant	RNF19A	GRCh38.p7	8:100261797	AAGTAAGTATGATTA[C/T]CAATTTTCTCCTTCT	25897
rs546578428	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100333243	GGCCCTCATCAGATG[C/T]GCCCACTCAACCTTG	25897
rs546617071	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325630	TATTTGCCATATCTT[A/G]GCCCCATCCCACAGT	25897
rs546691685	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280111	GAAATACAGTGAATT[A/G]GCCAGTCATTAAGGG	25897
rs546830524	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319286	CCAGCAAGAATATAA[A/G]TTTTTCTTAGGATGA	25897
rs546852870	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100266643	AGCTTCCTTAATAGC[A/G]GGGGCTACAGGCATG	25897
rs546999465	snp	C/T	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100333691	GGGCATGGTGGTGTC[C/T]CCTGTAGTCCTAGCT	25897
rs547013686	snp	C/G			downstream-variant-500B	RNF19A	GRCh38.p7	8:100256901	CAGGAAAAAAGGGTA[C/G]TTTCTAACACTGTTG	25897
rs547022104	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280900	AAATTATAATGGAAG[C/T]AAATGGTAAAAGTAA	25897
rs547049868	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289797	CCTAGAAAGGAATGC[A/G]TAAGAAAAATGAATG	25897
rs547077036	snp	C/T	0	0	intron-variant	RNF19A	GRCh38.p7	8:100272700	AGATGCACACCACCA[C/T]GCCTGGCTAATTTTT	25897
rs547253685	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	RNF19A	GRCh38.p7	8:100313343	GGTCTCTCAAACTAA[C/T]GTCAATTCTTCTGAC	25897
rs547273688	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100283568	AGTCCTAGCCCTCAA[A/G]AGAGTGGAAAGAATA	25897
rs547273819	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257250	ACTGCAGCCCATGGC[A/G]TTTTTCTTTTTACCA	25897
rs547295619	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305300	GCCTGACTTTCAATC[C/T]AACTCAATAACTCCA	25897
rs547373169	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267599	GGTCTTGAACTCCCA[C/G]CCTCAAGTGATCCTT	25897
rs547384182	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297332	GGTTCTATGATCTCT[A/T]CCAAGTAGTTTTATG	25897
rs547417131	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297905	TAGTGATAGAGTATA[C/T]TTTGTTGAGTGAGTA	25897
rs547427371	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314355	TATCATCAAGAATCC[C/T]TAAAGCTCCCAAATT	25897
rs547458390	snp	C/T	8.69014e-05	0.00659114	intron-variant	RNF19A	GRCh38.p7	8:100259255	GCCTTCTCTGAAATA[C/T]AAGAGTAACAAATAC	25897
rs547515664	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306905	AATTTAGCTATTCTC[C/T]GTAAGTAGTAAGATG	25897
rs547558932	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335330	AAAGATGTACTATTA[C/T]TATCCTCATTTTATC	25897
rs547584284	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100283532	ATTTTTAGAAATACC[A/G]TCCTTCAAACAAGTA	25897
rs547588311	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292521	AATGTAGAAATTTCA[A/G]AAGTTTTTAACGTGC	25897
rs547631774	snp	A/G	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274995	TAATGGATGAAGAAC[A/G]TATAGTTCTCAAACG	25897
rs547638572	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100327629	GTCATCCATGACTTT[A/G]TTGTGGTCATAACCT	25897
rs547676829	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293052	GCCATCTAGATCCCT[C/T]GAGTGCAGTTCGCAA	25897
rs547712503	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336421	CCGAACGACACTGAC[A/T]AGCACAGAGGCAAGG	25897
rs547764339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320979	CTAAAAAATACTAAT[A/G]ATCATCTGAGCCTTC	25897
rs547809251	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315014	AGGGAAACTGACATC[A/G]AGAAAATCACTCTAG	25897
rs547830627	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100322235	GAAAATCTGTTGTTT[A/G]GTATAGTCCCTTTTA	25897
rs547866934	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315758	AAGCGATCCTCCCAC[C/T]TCAGCCTCCTGAGTA	25897
rs547895511	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323037	ATGAGCACAGGCTGC[C/T]GAAAAATGTTGCCAA	25897
rs547902345	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329927	GAAAAATTTAAATAC[C/T]TTCCAAAATCATGAA	25897
rs547910687	in-del	-/C	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100315084	GGAGGCTGAGGCAAG[-/C]AGATGATTTGGGCCT	25897
rs548090333	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100319653	TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT	25897
rs548148578	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285422	AAAATCAAGTTCTTA[C/T]ACAAATTATAATTTG	25897
rs548164615	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310304	CCGCCCCGCTGCACC[C/G]GGGTGGCCCCGACTG	25897
rs548184344	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311858	TTACACTCTGTACAA[C/T]GGTAATATTTTCCAG	25897
rs548186322	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100283710	TAAAATTAATGTCAG[A/G]TACAGAAAATGTTCA	25897
rs548191671	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100259692	AACCACAAATCCACT[G/T]TATGATCTATACAGA	25897
rs548273187	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100308167	TAGTGAAAAAAATAC[A/C]CTAACATTAGTTGCC	25897
rs548350390	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100260222	CCAAGTAAAGTGGTA[A/G]TGAAATAACACAAAA	25897
rs548352643	snp	A/G	8.34105e-05	0.00645742	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269877	AGCTTACCTTAGATA[A/G]TGCAAATCTGAGATT	25897
rs548370180	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100317131	GGCCCGCAAGCGCCG[A/C]ACGCAGCCCAGCCCG	25897
rs548376923	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257780	CAATGGGGTACAAAC[A/T]TCCCCTTAGAGAAAG	25897
rs548377023	in-del	-/C			intron-variant	RNF19A	GRCh38.p7	8:100292217	AAAGAATAAAAAAAA[-/C]AAATTTAACTTTAAT	25897
rs548391402	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100260893	GGATGTCCTGACTCC[A/C]CCTGTTTCCCAGGAC	25897
rs548404387	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100309703	GCCCCGAGCCCACGC[C/T]GGACACTGGAGGAGA	25897
rs548405365	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100267179	AACTTAATCATGGAA[C/T]TTATATTAAGAATTC	25897
rs548413613	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290157	TCTGTGTCTGTTGCC[C/G]AGGCTGGAGTGCAGT	25897
rs548425078	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100334057	CATGCCTTTTCTTGA[C/T]TTTGCTCATTCTGTT	25897
rs548453926	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100286332	CGTATTTTGTTGTTA[A/T]CTATATTATAGTACA	25897
rs548517891	snp	G/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100262555	AGAGATGAGCTCAGA[G/T]ACATAGTTGGGGCAG	25897
rs548542101	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272264	GCAGTGCTGTCACAA[A/T]TTAAACACATATATA	25897
rs548568846	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293962	TCTTTTTCATAGTTT[A/C]CATTTCTCTGATGAG	25897
rs548579839	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100298063	CCTACAGTCCATAGA[-/T]TATAAAGATTAAATA	25897
rs548665244	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100296263	GCACGTGCCACCATG[C/T]CTGGCTAATTTTTGT	25897
rs548692424	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278352	ATATTAATATCTGAA[C/T]ACTCAAAATAAATAT	25897
rs548728941	snp	C/T	1.64741e-05	0.00286998	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287886	ACATTTCAGAATGTA[C/T]ACTTTCAATACTTGC	25897
rs548761873	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282570	ACTAGTCATGAATTA[C/T]AACTTCCCCTGAAAT	25897
rs548825586	snp	A/C/T	0.00518109	0.0506754	intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309341	AGGCCCCAGGCAGCA[A/C/T]GGCTTGCGGGGCGAT	25897
rs548849680	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100274819	ATAGGAAAGAATGAG[C/T]GCTTCTGGGATAGAA	25897
rs548850156	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325055	GGAATTACAGGTGCC[C/T]ACCACCACAACCGGC	25897
rs548857941	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289480	AATCAATAAGAAAAC[A/C]TAGACAATCCAATAG	25897
rs548884907	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317839	TGGCTTACACCTATT[A/G]TGGGGACCTGATTAT	25897
rs548972328	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318505	AAAAAAATGGGTGCT[A/C]ATTGTTATATAACTG	25897
rs548973166	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304052	ACCTCCACCTCTCAG[A/G]TTGGAGCAATTCTCC	25897
rs549052445	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312769	TCTCTATAAAAAATA[C/G]AAAAATTGGCTGGGC	25897
rs549069225	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326280	ATTCAATTCTCTTTA[A/T]ATGCATACCACCTAA	25897
rs549128615	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100273260	ACAATGTTATTGTTC[A/G]GCTAAAAGCATTTGG	25897
rs549165852	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297135	GTTGATTATTCCTTA[G/T]GAGGTAAGTCAATTA	25897
rs549253804	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280293	CAAAATATATCCCCC[A/G]AACTAGCAAATAATA	25897
rs549318904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100305800	TGCACATTTCACATA[A/G]TCTCATTTGTGATTA	25897
rs549399583	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335553	ATTTTTACTTTAATA[A/T]TTTTTAATGGAAATT	25897
rs549487365	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336223	GCGGCGAAGGTGATC[A/C]CGCACGTAAAGATTC	25897
rs549582578	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257468	AAAAGAAAATAATGC[C/T]AATCATACATGGACC	25897
rs549585310	in-del	-/A	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100286656	AAGTTGTAATTTGAT[-/A]AATGAAACTCACATC	25897
rs549653539	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275228	TCATTTCAAAAAGTA[A/T]CCAACTAAAGATTAT	25897
rs549667640	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320707	ATAGGGTTTCTATGT[G/T]GATTAGATAAAATAA	25897
rs549673975	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100312084	CACAAGCCAGAAACC[C/T]AGGATTGTTCCCAGG	25897
rs549690279	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100266989	TTTACAGAAGAAGAT[A/C]AACCTTATTCCCAGT	25897
rs549710192	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100259370	GAACACCTTAACGCA[G/T]AACACGTTCTACTTA	25897
rs549859602	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292301	AGCAAAGATATTTTT[A/C]GTATTGTCTCACTAC	25897
rs549905471	snp	A/C	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100313999	CAATCTTCCCCCCTC[A/C]GCCTCATGAGTAGCT	25897
rs549915465	snp	C/G	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100300577	AGGGTTGCTTGAGCC[C/G]AGGAATTCCAGGCTG	25897
rs549928628	snp	C/T	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100275974	AAAATAAAAAAAAAC[C/T]GTTTTTTTTTCCTTC	25897
rs549947129	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100284261	CTCATAATAAGTAAA[C/G]CTAACTTTTAATGAG	25897
rs549994255	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100321041	GGAGAGTCTTGCCTC[A/G]ATGTTGATGGTGGCT	25897
rs550102827	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277436	CCTGCCTCAGACTCC[C/T]GAGTAGCTGGGACTA	25897
rs550140788	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100329263	TATACACACATACAC[A/G]TACACAAACACACAC	25897
rs550172602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328004	TGAGGTAAGAGTCTC[A/G]CATCATGATGAGTCT	25897
rs550173392	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315622	TTCTTTCCCAGCAGG[A/G]TCATGGAAATTTTTC	25897
rs550205049	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316478	TGGTGCCTTTACAAT[C/T]CCTGAGCTAGATATA	25897
rs550205954	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100308676	TTAAAAAAATGAAAA[A/G]AACCATGTTCTTTAA	25897
rs550206590	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304981	TGCTCTGTTGCTCAG[A/G]CTGGAGTACAGTGGC	25897
rs550242287	snp	A/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100301346	CCTTCATTAATCACC[A/T]GGTATCCAAATTACC	25897
rs550243837	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317006	TACACTCTCCGCAGC[C/T]GCTGGCCCGGGTGCT	25897
rs550282916	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293139	ATAATGCTCACGGCT[C/G]CTCGCCTCCTGCTGC	25897
rs550329827	snp	A/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310420	GTGGCCCAGAGAGCG[A/T]CTCCTCCAAGGACAG	25897
rs550368284	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310935	TCTTAGTTGAATAAA[A/C]AAATTCCGTCTGGGC	25897
rs550370867	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100282379	AGAAGACATAGAAAA[A/T]GTGATTTTTAAACTT	25897
rs550371580	snp	A/G	0.00438332	0.0466095	intron-variant	RNF19A	GRCh38.p7	8:100271042	GTTCCAATGTCTTAC[A/G]TTATAAGCATTAAGC	25897
rs550509536	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323241	TTTTTATTTGAAGGT[A/C]GTATTTCATAGAAAG	25897
rs550593571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100331929	TAATATATCAGTACC[C/T]ACAAACTCACACAGT	25897
rs550600374	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303820	GCAGGTGCCTGTAAT[C/T]CCAGCTACTGGCAGG	25897
rs550654714	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100324818	TTTCTTCTTCCTTCC[C/T]TCCTTCCTTCCTCCT	25897
rs550745853	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100265982	TGGGAAACTTAGCAC[G/T]GAAGAAGAGAAAAGG	25897
rs550763999	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303264	CTGGTGACTATAAGC[A/G]TTCCTCGGCTTGCGG	25897
rs550773077	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285515	TACCAATCAATCTAG[C/T]ACAAGATAATATACA	25897
rs550852659	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325589	CACACCTCTAGCCTA[C/T]GCCCTGGGTCCTCAA	25897
rs550875138	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100272642	TCCTGGGGTCAAGCA[A/G]TCCTCCACTTCAATC	25897
rs550940539	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318664	GAAATGATTCCAAAC[A/G]AAAGCAAACAAACAA	25897
rs550964835	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100286538	CAGGCAGGAAACACT[A/G]CTTTTCTCATTTAAA	25897
rs550987501	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100313447	CGCAAAGGTCTTAGC[C/T]AGAAACACTTGTCAA	25897
rs551015477	snp	C/T	1.64798e-05	0.00287047	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288041	GATGAAGCAGAGGAC[C/T]GAAGATCTCGATCTG	25897
rs551050841	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100314219	ATACTATATATACTA[C/T]ATATAGTACACTATA	25897
rs551052329	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288862	TCAGGAGATTGACAC[A/C]ATCCTGGATAACACA	25897
rs551054187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279350	CACGTCAAACATTTA[A/G]TATTTGATTGCCAGG	25897
rs551151386	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100284933	TCAGTATACTAAGCA[G/T]GAACTGGAAATCAGA	25897
rs551167166	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301298	GAGCTAAAGGCTCAG[C/G]ATTCTTTCTACTATC	25897
rs551187950	snp	C/T	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100297251	TGTACAATCTAAATA[C/T]CTTTCAATTACTTCA	25897
rs551221749	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282648	TCCCATGTACTTGTT[G/T]TCTCTGGATAAAATC	25897
rs551222751	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289507	ATAGAAAAACGGGCA[A/G]GGGACTTAACAGGCA	25897
rs551260047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100264565	AGACTTACTGCAGGC[C/T]CAATTTAAATTGTCC	25897
rs551279455	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311998	TTGAATTCCTAGAGG[C/T]ACCTCAGATTCAGGC	25897
rs551340374	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274896	TTAACTTTAAAAAGT[C/T]AAAATAACTAGTGTT	25897
rs551401875	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100313570	TGGATGATTTAATAC[A/C]TTTTTAGGTATGGTA	25897
rs551408199	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305239	GAAAGACAGTAACGC[A/G]CAAAGTCATTTTGTG	25897
rs551441310	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319971	CTCCCAAGTAGCTGG[A/G]ATTACAGGTGCCCGC	25897
rs551463455	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100265771	GTGGGAGGTGGGTGA[C/T]GCATGTATGGGACAA	25897
rs551531107	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100306816	CTATCTACTAACAGA[A/G]AACTGGCATGGCTTA	25897
rs551576298	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100290344	TGACCTCAAGTGATC[C/T]GCCCGCCTTGGCCTC	25897
rs551716567	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326813	CAAACACAAAACTGT[A/G]TTTGACTCTCTTTGA	25897
rs551747561	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336350	TAGGTCAGGAGCTGC[A/C]AGTTTGCAAATTCCA	25897
rs551784641	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336987	AGGATGTAAGTTAAA[C/T]CTTAATACAGTTGTT	25897
rs551798985	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320538	AGGTGCTAATATTCA[A/C]TGGGTGGAAAAATAA	25897
rs551836211	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314267	ACACATACTATATAT[A/C]CTTTTTATTGAGTAC	25897
rs551872664	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329120	AGGGAGAGGGGTGGT[A/G]TAGCTTACAGACACC	25897
rs552005099	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100325193	GATTATAGGCATGAG[A/C]CACTGCGCCCAGCTT	25897
rs552005475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100321123	TAAAATAAGATAACA[A/G]TGAAGTTTGCCACAT	25897
rs552088540	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292438	TGCTATCATATGGGT[A/G]TGTGTGTGTGTGTGT	25897
rs552120465	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100307341	CAGCACTTGACTAGG[A/G]ACTTTTACATGTTAT	25897
rs552159373	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100333632	GTGTTGCCTGGGCAA[A/C/G]ATAGCAAGAGCCCAT	25897
rs552167199	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100316316	TTTACTGCAAAGAGC[A/G]AAAGAACGAAGCTTC	25897
rs552174189	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100284446	CACAAAAGTAATCTC[C/T]GTGACTTTTTTTCCT	25897
rs552303358	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100322169	TGACTTCTCCTCTCT[A/G]TGAAGTCCAAATGGC	25897
rs552339982	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100276353	TTACATACTGTATGA[A/T]TCCATTTATATATTT	25897
rs552378215	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277473	CCCACTACCACGCCC[A/G]GCTAATTTTTTTGCA	25897
rs552477697	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100308790	AACACTTAAAATTAG[C/G]ATTTCTAGCCAACAT	25897
rs552521110	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287126	AAAAAATAAAGAAGG[C/T]CATTTGAATTTATGA	25897
rs552569540	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301447	AGTTTCCTGTGGCAT[C/T]AAAAGCCCTCCACAG	25897
rs552615503	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100261103	ACCACCAAATTTTTC[-/T]TTTTTTTTTTTGAGA	25897
rs552626306	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303277	GCATTCCTCGGCTTG[C/T]GGTTACATCACTCCA	25897
rs552626628	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294201	GAGGCTCTGTAGTCT[C/G]TTGTCTTCTCCTGAA	25897
rs552644976	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100290962	TCCAACCAGAAGCCA[A/G]CTGCCTCTAAGGCAG	25897
rs552645272	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100310132	CCCCCGCTTTCCCCT[C/T]CTCCTCCTCCCACTT	25897
rs552663588	in-del	-/AA			intron-variant	RNF19A	GRCh38.p7	8:100262539	AAATAAGAGGGTGAC[-/AA]GAGATGAGCTCAGAG	25897
rs552696844	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100275899	ATGTATGCAGAAGTC[A/G]CACATTTTTCTTCCT	25897
rs552712583	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294864	ATCCTTTAAAAGATT[G/T]TCTTGCATTATTCAA	25897
rs552795009	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330134	GTTTCCATCCAAACA[A/C]CATCCCTTCCACTTC	25897
rs552848894	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100324614	TCTTTTAATTAGGCT[C/T]CTAACATACATTTGC	25897
rs552849015	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100332140	AAAAGTGGAATTGCT[A/G]GTTTAAAGGATATGT	25897
rs552892984	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287324	ACGATATAGAAATGA[A/G]TAAGATAGGATCACT	25897
rs552921734	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100324134	ACACACTGAAGCTGC[C/T]ACTATAATTTATTTT	25897
rs552961396	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100274904	AAAAAGTTAAAATAA[C/G]TAGTGTTTTGTGTCA	25897
rs552982573	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100278798	AATGAATTAAGTTTT[A/T]AAAAAAAGTACTTCT	25897
rs553097947	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286814	TTCCTGAATAGTATA[A/T]GACTACTGTTTCCCT	25897
rs553119753	snp	C/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100318174	CTTTGGTTTTAGCAC[C/G]TGGTATAGTTGTGTT	25897
rs553172227	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316337	ACGAAGCTTCCACAG[C/T]GTGGAAGGGGACCCC	25897
rs553259506	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279555	ATTTTTGTACTTTTA[C/T]TTTTTATTTACTTTT	25897
rs553322800	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317421	ATCTCTCACTGGGCC[A/C]TTCAGAGAGTGCCAG	25897
rs553339080	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271584	ACTGAAAGGTAACAT[C/T]CCCATTTATTCTTAT	25897
rs553426191	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100262149	AAGCTATTATTAAGA[C/T]CTGATAACACTATGT	25897
rs553426258	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272177	CAAAAATGAAAAATA[C/T]GTGGTTCATTTAAAA	25897
rs553448083	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272857	GCCCAGCCCTCACTG[A/C]ATTTCTAATTCTTCC	25897
rs553482520	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100312150	CCACCAAGTCCTGTT[C/T]ATTATACCCCGGAAA	25897
rs553485192	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100273734	ATGAGCCAGGAACTA[C/T]TTCAACTATATGGAC	25897
rs553492197	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280514	TTTTTAAATGGAAAA[A/G]GTAAGATGTCCTACC	25897
rs553559225	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304413	GTACTATATACATCA[C/T]ATACCCTAAGATAAC	25897
rs553574731	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100264992	TTGCTTAAGACAGTG[A/T]TTTAATGGATTTTAC	25897
rs553645871	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304907	CATAATTAACTTATA[C/T]TAATCCAATGAAAAA	25897
rs553646093	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100295777	AGCTAATTTTGGCCC[A/T]AAGTAAACAGAGTTT	25897
rs553711901	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100312908	GCCTGGGCAATAGAG[C/T]GAGACTCTGTCTCAA	25897
rs553790188	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100298466	ATATCATTAGTGTAG[A/G]TGAGTATCAGTTTCC	25897
rs553822920	in-del	-/G	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100275975	AAATAAAAAAAAACT[-/G]TTTTTTTTTCCTTCG	25897
rs553823041	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100281418	CTTAATTTACTTAAA[C/T]TAAGTCATTTATAAT	25897
rs553828697	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100299672	GCTGAGGCAGAAGAA[C/T]TGCTTGAACCCAGGA	25897
rs553829165	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100290802	ATACTGTATAGATTA[C/T]TGCTCCTAGGCTACA	25897
rs553914172	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291615	ACACATCATTAGAAA[A/G]GTATTCTGGAAATGA	25897
rs553953052	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100331997	ACACCATATATTAAC[A/T]AAATAATTTCCTATT	25897
rs554036417	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319994	GTGCCCGCCACCATG[A/C]CTGGCTAATTTTTGT	25897
rs554079314	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272701	GATGCACACCACCAC[A/G]CCTGGCTAATTTTTG	25897
rs554104331	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100321454	AGGCTCCACTTCCAA[C/T]TCTAGTTCTCTTGCT	25897
rs554228436	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314775	CTCCACAACAACCAT[C/G]CTTACCTCTATAATT	25897
rs554314965	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100297134	AGTTGATTATTCCTT[A/C]TGAGGTAAGTCAATT	25897
rs554348145	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284002	GCTTCAATAGGTCAG[A/G]GATTTTTGTCTTGTG	25897
rs554378221	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100322854	TCAGAACACACACAC[A/C]CATTTATTAAGTTCA	25897
rs554399315	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100302666	AGAGTAGGGAATGAG[G/T]TCTGTAGCATCCCAA	25897
rs554414728	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100335500	AAAAAGAAACCCAAG[C/T]TGTCCCAAATATGAG	25897
rs554508750	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301477	GTGCAACCTCAGTTT[C/T]TCACTGTTCTACATA	25897
rs554538807	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267150	CCATGACTGAGTTCC[C/T]AAATAGCTACTGAAA	25897
rs554619911	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100302139	TATTCTAAGTGAGAC[-/A]GGGAAACTTGGGTTT	25897
rs554624353	snp	A/G	4.94214e-05	0.00497074	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258949	GAGGGATGGAGCCTC[A/G]AATTCACTTGAGTTC	25897
rs554632431	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100308211	TCCTCAAAGACACCT[C/T]GCGATGACATTAAAA	25897
rs554637976	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269609	AAAGTATTTATGGGT[C/G]TAGCATAATTACACA	25897
rs554776093	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100300758	TAGATGTATCAGATA[C/T]TTAACTAGTCAACTC	25897
rs554799520	snp	G/T			downstream-variant-500B	RNF19A	GRCh38.p7	8:100256659	ATTTCATAATCTAAT[G/T]TTGCTAGAATAGAAT	25897
rs554864978	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337659	GAGATTTTGGCAGGG[A/G]TGAAATGACTGGCAT	25897
rs554884422	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100293193	CACACTGTGGCCCAA[A/G]GGTTGGGGAGCCCTG	25897
rs554900187	snp	A/G			missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287543	CAATCAGGATCTGCA[A/G]CAAGCCACCGTCTAA	25897
rs554938834	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100285744	TTCAAGTTACCTTCC[A/C]GTCTTGGCCTCTCAA	25897
rs554949703	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310709	ACTTAGCCACAATAG[A/C]AAGCCTACGTGAGGG	25897
rs554952444	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100294956	CTCCAAGTAACCTGT[A/G]TAAGTATTAATTCAT	25897
rs554952709	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100267512	GTAGCTGGGACTACA[A/G]GTGCATACTACCATA	25897
rs554955989	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276890	AGTAAATCAGGAAAT[C/T]TGAGTGAGATTGGTA	25897
rs555007798	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286509	AGTGATACCTGGGAA[A/T]ATTGGGATTTGCACA	25897
rs555034723	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303336	CTCCTTTTCTGCGCG[A/T]CGTCTTCTCTGTAAT	25897
rs555040134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100295677	TGTAGTAGCTGACTA[C/T]CAAAAAATAGATAAT	25897
rs555079788	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100260134	TTTATTTCCTTTTAT[C/T]TAATTTAAATTCTAC	25897
rs555079868	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293659	CAAATACAGGAATTC[A/G]GGGAAAATTATTTCT	25897
rs555083283	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100275409	TTTTTAGGTTCAGGG[-/T]TTTTTTTTTTAGATT	25897
rs555193312	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310180	CCGCCCCGCCCCAGC[A/G]CGCCGCCCGCGTGCT	25897
rs555196203	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100328003	TTGAGGTAAGAGTCT[C/T]GCATCATGATGAGTC	25897
rs555249139	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100317128	GCTGGCCCGCAAGCG[C/T]CGCACGCAGCCCAGC	25897
rs555268568	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100332359	TTATAAGTGTCTGGC[A/T]TTTCCCTTGTTTGCA	25897
rs555299034	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311551	GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA	25897
rs555303326	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318813	ATGGTTTCACCCTCA[A/G]AGTGAAATCCTGTGC	25897
rs555327385	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100280756	AACAGTATTAGGCAC[A/G]TTCTGTAATATATCA	25897
rs555391224	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312257	TCCACGTTGCACCCA[A/G]CAATTAAATCAGAAT	25897
rs555448684	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100331530	CAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	25897
rs555470928	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278876	AATTTCATGACAAGT[C/T]CCAAAATCTGGTACA	25897
rs555562004	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305012	ACAATCTCAGCTCAC[C/T]GCAACCTCTACCTCC	25897
rs555565811	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100291459	CTTTTACCTTCAGAA[G/T]TGCTTCAGGATTCGT	25897
rs555650308	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100296659	GGAGTCTAAAGTACA[A/C]TGAAAGGTTAACTGT	25897
rs555665114	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272744	AGACGGGATTTCACC[A/G]TGTTGCCCAGGCTGT	25897
rs555704910	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100320156	GGTTCACATTTTTAT[A/G]CTTCTACAACATAAG	25897
rs555898968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100305410	TCTGCAGAAAGAAAC[A/G]TGTCATACAAAACGC	25897
rs555902655	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100273827	TCACTCTGTCATCCA[A/G]GCTGGAGGGCAGTGG	25897
rs555917982	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257937	AAACAAGATAGAGTA[C/T]CAGGTATTTCTATTT	25897
rs556092227	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289860	CTCACAATAGCATTA[G/T]TAATAATATTCAAAA	25897
rs556155169	snp	C/T	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100290800	GTATACTGTATAGAT[C/T]ATTGCTCCTAGGCTA	25897
rs556214797	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282965	GTTGATCACATTACC[A/C]AAATGTATATGAGTT	25897
rs556229103	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100319691	CACACCACCATGCCC[A/G]GCTAATTTTTGTATT	25897
rs556273030	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284572	TAATCACGTGGTTGT[C/T]TTCATAGTAACAGAG	25897
rs556351429	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100313799	GGTGGAGACTGTGGA[A/G]ACAGAAGTGGATGGT	25897
rs556387187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328503	TTGAGACAGAGTCTC[A/G]CTCTGTCACCTAGGC	25897
rs556394091	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276468	TATAAGAGAGCAACA[C/T]AGGCCAGGCATGGTG	25897
rs556410747	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307026	CTATGATGTGCTAGT[C/T]TGCCAAATACAATGC	25897
rs556460630	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315428	AGGAATGAATGGGAG[C/T]TTGGGGGCTTTAGTC	25897
rs556487736	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100334551	ATAAGTATCTGGGGA[C/G]CTTTAAAAAATATGG	25897
rs556494794	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100299755	AAGAGCAAAACTCTG[C/T]CTCAAAATAAAAAAA	25897
rs556499324	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100308350	TTTTAGCATAATTTG[G/T]TTTATTAAGTCCCAA	25897
rs556587279	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100309128	AAAACTGAAAATTCA[A/G]AGTAGTAGTATTACT	25897
rs556600471	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100322407	CTTCTGAAGCTTCCT[C/T]ACCTCTCAGCTTTCA	25897
rs556620963	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100309809	CCTGGGTCGTAAGCG[A/T]GAGCCGCCCCTTCTC	25897
rs556624749	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100269286	TGCAAAACATGCATA[C/T]TTTTAGGCATCAATT	25897
rs556701697	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336550	TTCATGAGACTTCTC[A/G]CTCTTGAAGCTCCTG	25897
rs556733748	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276098	TCTAGGCATTCTTTG[C/G]CATTTATCCCAAACA	25897
rs556841942	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330544	GTTAATTGCAAAGCT[A/G]GAGTTGCCAGAAGCC	25897
rs556852510	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302603	CTGTTATTTGGATGG[G/T]ATGTAAAATCGTGAA	25897
rs556895827	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100276401	TTAGTGGTTGCCAAG[A/G]ATTAGGAATGGGGAC	25897
rs556919792	snp	A/G	4.94246e-05	0.0049709	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287961	TATCTTTTTTCCTCC[A/G]AAACAGGGAGCCTAT	25897
rs556929770	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100331252	AGTGGCCGTCCTTTT[A/G]AACCTTGATTTCACA	25897
rs556939026	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100259721	GATTTGCCTACTCTG[A/G]ACAGCTCACTGTTTC	25897
rs556980246	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328664	TTCAGTAGAGACGGG[A/G]TTTCACCATGTTGGT	25897
rs557052463	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100275964	CTCCTGCCAAAAAAT[A/T]AAAAAAAACTGTTTT	25897
rs557094474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293318	TTCTTTCAACTTTTA[C/T]CTGGGGAAAAAAAAT	25897
rs557106525	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100324363	ATGACTAAAGTTGAT[G/T]ATTAATCACAAAGAA	25897
rs557192115	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317245	CTCACAGTGCAGTGG[C/T]GGGCTGAAGGGCTCC	25897
rs557204245	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100285789	AGGAATGAGCCACCA[C/T]GCCCAGTTGTAGATT	25897
rs557269555	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258142	CAGTTCTTTTAAACT[C/T]ATCTCTTTAGTGGTT	25897
rs557290020	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100286755	AATCTCTGGTTTACT[A/G]ATAGTATGCTACGTA	25897
rs557339700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270642	AATCAGTACCCAAAA[C/T]ACAAGGAAGGAAGGA	25897
rs557430884	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279699	TGGCTAATTTTTTTT[C/G]TATCTTTAGTAGACA	25897
rs557441681	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100295739	CTTAAAGTGATCTAC[C/T]AGAAATGATGTATTT	25897
rs557545398	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100272825	AAAGTGCTGGAATTA[C/T]AGGCATAAGCCACTG	25897
rs557628092	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303511	TAGGACATGAACATA[C/T]CTTTTGTGGGGTTAC	25897
rs557634285	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311308	GTTTTAAAGCTGTTA[C/T]ACCTTTAAATGCTAC	25897
rs557659624	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325838	ATAACACGTCAAGCA[A/G]GACTTTAACTCATTT	25897
rs557671303	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304206	ACCTCAGGTGATTTG[C/T]CCACCTTGGCCTCCC	25897
rs557685718	snp	A/C	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100312863	GGAGGCAGAGGTTGC[A/C]GCGAGCTGAGATTGT	25897
rs557717353	snp	A/G	0.000253141	0.0112475	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264185	AGCTAACATAATAGG[A/G]ACACCGATACCTAAA	25897
rs557745475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100296407	ACCACGACCAGCCTC[C/T]GGGCATTATTCTTAC	25897
rs557808528	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100305988	GGAAACCTAACATCA[C/T]CACATTCCCAAAAGC	25897
rs557852912	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100332505	CCTTTATAAATTACT[C/T]AGTTTCAGGGAAGTT	25897
rs557890054	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100333404	ATCTATACCAAGGAA[A/G]TTCACATAGCTACAA	25897
rs557917446	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100286697	CTCTGAGATTATACC[C/G]AGATAATCTTGGAAG	25897
rs557957010	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280507	TCAGTATTTTTTAAA[C/T]GGAAAAGGTAAGATG	25897
rs558033788	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335739	TTGGGTCACTCTTAC[C/T]CAGTGCACTGGACAG	25897
rs558095235	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100318759	ATGCAACAAAGAACA[C/G]TCACTACCGGATTTA	25897
rs558121898	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100328027	ATGAGTCTGAGAACT[C/T]AGTTCTTTTATAAGA	25897
rs558175214	in-del	-/T	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100327122	GGTTTGGTTTTTCTG[-/T]TTTTAATCTTAGCCT	25897
rs558232235	snp	C/T	0.00398564	0.0444627	intron-variant	RNF19A	GRCh38.p7	8:100294549	TAACTCCCTCCTTTC[C/T]GCGATTTATCCTATT	25897
rs558281769	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100266316	CATGTTTGAAAAAAG[C/G]AGATCTGTAACTGTA	25897
rs558296402	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100298348	AAATTATATAAATAA[C/T]GTACAGCTAGTACAA	25897
rs558331952	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100290655	AGAGAGCTCAATCTA[C/T]ACAAATACAGTTATG	25897
rs558333941	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100263272	TATGGTAAGAAGTGG[-/T]TTTCCCATAAGAAAA	25897
rs558356672	in-del	-/TGGA	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304982	CTCTGTTGCTCAGGC[-/TGGA]TGGAGTACAGTGGCA	25897
rs558452256	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100259481	TGTTCTAGACACTAT[A/G]CTACCTTTTTTTAAA	25897
rs558501701	snp	A/C			missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264736	CCACCTGCTATGGCC[A/C]AATTCCGTTTGTGCT	25897
rs558519702	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100320370	TATTCATTTTGACTG[C/T]AATGTAAATACACAT	25897
rs558573248	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267047	AAAGGAAACAAAAGG[A/C]AACAGATCTGACTCA	25897
rs558603471	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100334890	TGTCTGCACTGGGGC[A/C]TGCTCTGAAGGTTGC	25897
rs558624715	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276153	AACTTGTACACTAAT[A/G]TTCAAAGCAGCCTTA	25897
rs558644467	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100332430	TCTCGTTCCACCATG[A/G]TTGTAAGTTTTCTGA	25897
rs558663351	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100276595	CATCTCTACAAAAAA[C/T]ATTTAAAAAATTAGC	25897
rs558680967	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293180	TCCTAACAGGCCACA[C/T]ACTGTGGCCCAAGGG	25897
rs558684913	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100276795	TGGAACTGTTCAGTA[C/T]CTTGACTGTGGTGGT	25897
rs558772182	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100285592	ATATCTCCTGGCCAA[A/G]GGCTGTGACAACTTA	25897
rs558877877	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292764	CCCCTACATACATAC[G/T]GATTTAATTTTTTAA	25897
rs558883928	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100312425	CCTGAGCAAGATGGC[A/G]AAAATACAAAAATTA	25897
rs559019318	in-del	-/TC	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100324861	CCTCCCTCCTTCCTT[-/TC]TCTCTTTCTCTTTTT	25897
rs559034103	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329748	GTCTTCCAACACTTA[A/C]AGGATCGTCTGATGA	25897
rs559041396	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100300262	GAAAAGGGAGTATTT[G/T]CTAAAGACAGAAAAA	25897
rs559121693	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100322958	ATCACCATAACAGAT[A/G]TAATAATAACTTAAA	25897
rs559127304	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293392	GAACTCCAGGTTGAT[A/C]TCTTTATCCTTTCAG	25897
rs559131130	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100316154	TCGCGGTGAGTGTTA[C/T]AGCTCTTAAGACGGC	25897
rs559135589	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100338009	TTTGAGACAGAATAT[C/T]ACTCTGTCACCCAGG	25897
rs559161929	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100285952	GAACTCTTGCTATGG[A/G]AGTATTTGTTATAAT	25897
rs559165381	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100260382	TCCAAAAATCCTGGG[C/T]ATCTATATTAAAAAA	25897
rs559185393	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323641	ATGTGTTAGAGGAAG[A/G]CATATTTAAATAGTA	25897
rs559287084	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337106	GCATTTCTTGTTTAC[G/T]TTTTTACTTTTGGCT	25897
rs559341660	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100285169	CTAGGAGTTGAAATT[C/T]TCAGTTGTAGAATAA	25897
rs559454479	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100278659	CAAGGCAGATTAATA[-/G]AAATTAGATTACATA	25897
rs559465622	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100319208	AGTTAAACCTGCTTC[A/G]AAAAAATTTGTAAGC	25897
rs559478441	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310263	GCTGTTCCCTTGCGC[A/G]CGTTCGTTCCGCGCC	25897
rs559596597	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269802	AAAACCCAAATTTAA[A/G]ACAAGTTATTTTGTC	25897
rs559684334	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270692	TATGGCTATGAACGT[C/T]ATAAACCATGGAAAA	25897
rs559689058	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271834	TTTCTCTCCAAATAC[C/T]CTCATGATGCAAAAA	25897
rs559714821	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100277121	ATCAAGTTTTATCAA[C/T]GCATGTCTTTTGTAA	25897
rs559739220	snp	C/T	0.000399281	0.0141238	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287716	GCAATCCACACAAGA[C/T]CTGTGATGACAAGTC	25897
rs559758002	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335847	ACAGCAGTGCTCTGG[C/T]CTAAGTGGGCCAGGC	25897
rs559775927	snp	C/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100279312	AGCTGGTAGTGTAGG[C/G]GAAATTACTAATCCT	25897
rs559859578	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100335963	GAACCAACGGGACAA[G/T]TTTAGCCAAAAATGG	25897
rs559873980	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304546	CTCCACTTTCCAAAT[A/G]ACCTTATTTCATGAT	25897
rs559897681	snp	C/G	0.00318978	0.0398085	intron-variant	RNF19A	GRCh38.p7	8:100302376	AAGAGGATTTGGCCT[C/G]ATTAATCAGAAGGCT	25897
rs559903549	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303610	GCAAAAATCTAAAGG[A/T]TATTTAACGTTTGTG	25897
rs559940450	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100295314	ACTTTAGATACTTTT[A/G]ACAGCACTCTATTTT	25897
rs559975634	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288731	ATGCCACAAGGATGA[A/C]TACAAAGACCAGTGG	25897
rs559976282	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100300307	ACACAGCAGGTAAAC[A/G]ATCATAAAGGTTTAT	25897
rs560085111	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289426	GCCACATATAACTAA[C/T]AAAGGCACAGTGCCC	25897
rs560099164	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325031	CCTGCCTCAGCCTCT[C/T]GAGTAGCTGGAATTA	25897
rs560156609	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290215	CATCTTTTGGGTTCA[A/G]GCAATTCTCCTGCCT	25897
rs560188964	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325424	TTTGCCCCTCTGTTT[A/T]ACCTGGCCAGTTTCA	25897
rs560223227	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326695	ATGAGCTCTTGAATT[A/C]ATTCCCTTCTTCCCT	25897
rs560351452	snp	A/C	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100320323	AACACTATTTTCAAG[A/C]TCTACCCATGTTGAT	25897
rs560356788	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271663	AGAATTAATACCACA[A/T]GCAATGTATTTTTGA	25897
rs560446738	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100326800	AAACAGTCTGTATCA[A/G]ACACAAAACTGTATT	25897
rs560527158	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274667	TGGGATTACAGGAGT[A/G]AGCTACCATACCTGG	25897
rs560559022	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100313429	AGACGGAGGAACAGC[A/G]GACGCAAAGGTCTTA	25897
rs560616291	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282209	TGGTTTTGAATGAGG[G/T]TGAAGGGGAAGAATG	25897
rs560656160	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100264935	CCTACTAGTGTCCTT[A/C/G]AACTATTATATATTC	25897
rs560724118	snp	C/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336349	ATAGGTCAGGAGCTG[C/T]CAGTTTGCAAATTCC	25897
rs560762053	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100266377	CTCTTCTCTATAAAT[G/T]ATTTATAGGTACATG	25897
rs560801131	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258144	GTTCTTTTAAACTTA[C/T]CTCTTTAGTGGTTTC	25897
rs560857765	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100267439	AAGTGGCACAATCAC[A/G]GCTCACTGCAGCCTC	25897
rs560865231	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314088	GGTTTTGCCATGTCG[C/T]TCAGGTGGGTCTTGA	25897
rs560880088	snp	C/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100267624	ATCCTTCTGCCTCAG[C/G]CTCCCAAAGTGCTAC	25897
rs560889585	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100284783	ATCACATATAAAAAA[A/G/T]GTTTATAAAGAATAG	25897
rs560898245	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306675	CCAAAGTGATTTCAC[G/T]GCCTGTTTGGTTGAA	25897
rs560926255	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100281727	AAAGCATAAAGCTTT[C/T]AACATACCTTTAAAT	25897
rs560948866	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291364	TGAATGAATGATGCT[C/T]TTCAGTTGCTATTAC	25897
rs560948894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100299985	ATGTAATTGAATGAT[A/G]TATGTACATAGGAGA	25897
rs560964124	snp	A/C	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100268627	TGCCAAACACTAAAA[A/C]TTTATGAAAAAAGAG	25897
rs561014323	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100306454	ATAGGATAAGACTAC[A/G]TAATGGTTTTAAGGC	25897
rs561034055	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100292187	TTCAGCACATGCTTA[C/T]GTTGAGAAGATAATA	25897
rs561079285	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100260514	GCCTCAAGCTATCCT[C/T]CCAACCTGGCCTCCC	25897
rs561208609	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328620	GGGATTACAGGCACG[C/T]GCCACCACACCCAGC	25897
rs561281800	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309327	AGCTCCCCTCCCTAA[A/G]GCCCCAGGCAGCACG	25897
rs561317109	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294345	ACCAATCCCTTCTAT[C/T]TTGCTGGGAATCAAA	25897
rs561319296	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286136	GATTCAATCGCATCT[A/G]AGCTGTTTTTCTGTC	25897
rs561355489	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287037	ATGAACACATCATAC[G/T]GTGGCACATGCTAAG	25897
rs561453571	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304583	TAAGGATGCCTATAT[A/G]AAAAGTCCCATTTAT	25897
rs561454427	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323816	AACTTGTTGAAATTC[A/C]TACTTGGGAGTTTTC	25897
rs561458560	snp	A/C	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100308564	AAATGTGTATTAAGA[A/C]GGGTAATGGCAAAAC	25897
rs561494837	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301303	AAAGGCTCAGCATTC[C/T]TTCTACTATCTTACT	25897
rs561517292	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100332705	CAAATTTGTTAAAAT[G/T]TTATCTCATTTTCAT	25897
rs561574314	in-del	-/A	0.00517822	0.0506191	downstream-variant-500B	RNF19A	GRCh38.p7	8:100256566	ATACCAGGGAAACAG[-/A]AAAACCATCTATGCA	25897
rs561578696	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100317467	TTCTTCCTCTTCATG[A/G]GACCCATGCAATTAC	25897
rs561598109	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330854	CTTCATCTCTCTCCA[C/G]AACCCTCTTGAGACT	25897
rs561624585	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278086	GTAATTTTAAGTAAA[C/T]TACATTATCTCCCAA	25897
rs561657175	snp	A/T	0.00597247	0.0543191	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100338124	GCTGGGACTACAGGC[A/T]CCCACTACCACGCCC	25897
rs561728416	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277287	AGGGAGTTCCCTCCA[C/T]TTTTGGACTTGTTGA	25897
rs561844793	in-del	-/C	0.00478085	0.0486577	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336752	TGTTTTTTTTTTTTT[-/C]TTCTTCTTTGGAATT	25897
rs561854122	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310932	TATTCTTAGTTGAAT[A/T]AACAAATTCCGTCTG	25897
rs561879661	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100292381	GCTGCAGCACTTTTC[C/T]TTACTGATGTGTAAG	25897
rs561894733	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303627	ATTTAACGTTTGTGC[A/G]TAATTTTAAAAATGG	25897
rs561916881	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100324685	CTAAATATGAATCTA[C/T]GCGTTTGCTTCAAGA	25897
rs561937365	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271648	CTAAAATCACACATG[A/G]GAATTAATACCACAA	25897
rs561950889	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310311	GCTGCACCCGGGTGG[C/T]CCCGACTGCGGCCCC	25897
rs561968902	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100319799	CCTCCCAAAGTGCTG[G/T]GATTACAGGCGTGAG	25897
rs562113697	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100295441	TACAGAATATTCATT[A/T]TGCTCACTGGGCATA	25897
rs562122641	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100332901	GCCTCTTTTCTATCA[C/T]ATGTGTTTCAATTTT	25897
rs562150378	snp	C/T	0.000399281	0.0141238	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287946	TTGATTTACGTTTGT[C/T]ATCTTTTTTCCTCCG	25897
rs562161763	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304470	TTCCCCACTTACGCA[C/T]TCACACTACTTACCA	25897
rs562198498	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100295869	CACTTTCTCTTAACA[A/G]AGAGAAATCACTGAA	25897
rs562214477	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325556	AATTTGGATCTAGTT[A/C]TCTGCCCTCAGCAGC	25897
rs562238967	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288789	ATATAGGCCAGGCGC[A/G]GTGGCTCACGCCTGT	25897
rs562359004	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100301033	ATCTAACCTATTTTT[A/G]TAAGTGAGAAAACTG	25897
rs562396257	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100327276	TTTTTTTTTGAGACA[C/G]AGTCTCACTCTGTCG	25897
rs562413474	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326025	TATATGCTATCTGCT[A/G]TCCGGGTGTTTTATG	25897
rs562414585	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100283696	ACTGTATGTTTAAGT[A/T]AAATTAATGTCAGAT	25897
rs562427433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100290321	TGGTCAGGCTGGCCT[C/T]GAACTCCTGACCTCA	25897
rs562434039	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272972	CTAGGCTCAAACGAT[C/T]CTCCCACCTCAGCCT	25897
rs562467791	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305213	GCTGGGATTACAGGA[C/T]TATACATTGGGAAAG	25897
rs562515909	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100290970	GAAGCCAACTGCCTC[C/T]AAGGCAGTCCTTAGA	25897
rs562516759	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100329535	GAAGTCAATGGTCCC[A/G]CTGAACTCAGCAATG	25897
rs562552441	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283232	GGCCTTAGCCAACTG[A/T]AACAGGTGATAGAAA	25897
rs562645302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325133	GGCTGGTCTCGAACT[C/T]CTGACCTCAGGTGAT	25897
rs562663621	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100305574	GAAAATTTTAAATTA[C/T]ATTTGTGGCTCACAT	25897
rs562720041	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326775	AAGTGATACTTATCT[C/T]AAACACTTTAAACAG	25897
rs562771175	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314825	ATTGTCATTATTTGT[A/C]GGCCTTTCCCACTAA	25897
rs562828321	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100303044	CATGATATAAAACAA[C/T]GATAATTAGAGATTT	25897
rs562932091	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320906	ATTGTGGGCTATTAA[A/G]TGTGCAATAGCATCA	25897
rs562989748	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274782	CAGTATAATCTTTCT[A/G]ATTTCAGAACCACTT	25897
rs562996222	in-del	-/GAT			intron-variant	RNF19A	GRCh38.p7	8:100295111	TGAACAGATACTTCA[-/GAT]GATATCTTCTCCAAA	25897
rs563025472	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100266549	AGGGTCTCTCTGTGT[C/T]GCTCAGACTAGAGTG	25897
rs563127836	snp	C/T	0.00095544	0.0218359	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259145	CCGCCAGCATGACTT[C/T]GGGTGGCACTGCCAT	25897
rs563184502	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100300946	GCTCATGTACTTACT[C/T]GCTCTTCTCAAGAGG	25897
rs563224073	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292949	TGGTACCAGGACCAA[C/T]TTCATAGAAGACAAT	25897
rs563228012	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285799	CACCACGCCCAGTTG[C/T]AGATTTTTTTTAAGC	25897
rs563256320	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100300179	ATTAGCTTCTCTTTA[C/G]ACAAGTCTCCCGAAA	25897
rs563345106	snp	C/T	0.00716266	0.059414	intron-variant	RNF19A	GRCh38.p7	8:100292357	GCACTAGGCACATGT[C/T]TATATCCTGCTGCAG	25897
rs563359892	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284369	AAACCTACATCACCA[A/G]GTATGTGAAATACGA	25897
rs563378504	in-del	-/C	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100281048	CTCTGACTCAAACAG[-/C]CCCCAGACCTTAGTT	25897
rs563403371	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329708	TACTTGGCTAAGAGA[A/G]AAAAGACTAGAGCAG	25897
rs563425221	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285105	ATTGTGGAACATCCC[C/T]GTACAAATCTCCTGG	25897
rs563446499	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100285008	GAAGTTCACATCCCC[C/T]CTTCCTACTCTCAAG	25897
rs563473224	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276325	CCGAGTGAAAAAAGT[C/G]AATCTCAAAATGTTA	25897
rs563513208	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272328	AACACAAATATTAAT[A/G]TACTTTATGTAACTA	25897
rs563517527	in-del	-/AAGCGTGAGCCA	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100279515	AGTAACTGAGATTAC[-/AAGCGTGAGCCA]CCAGACCTGGCCAAT	25897
rs563545480	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100260577	GCCCAACCAACATTT[G/T]CCTTTTTAAAAAGAG	25897
rs563563103	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100277063	TAAAACTTTCAATTT[A/G]AAAATTTCTAGAAGT	25897
rs563567404	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100322115	ATTAGCCCCTAAGGA[A/G]AGAGTCAGCCTCTCC	25897
rs563579445	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315646	ATTTTTCTTCTTCGT[C/T]GTCTTGTTGTTGTTG	25897
rs563595088	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335855	GCTCTGGTCTAAGTG[A/G]GCCAGGCTGCCCCTC	25897
rs563621904	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100316077	ATGGTCAGATGTGTT[C/T]GGAGTTTCTTCTTTC	25897
rs563702907	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309361	TGCGGGGCGATGTCC[C/G]GGCTCCAAATTTGCA	25897
rs563743045	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100297656	GAGGCAGAACTTAGA[A/G]GACAGAGGAGTCACA	25897
rs563750741	snp	C/T	0	0	intron-variant	RNF19A	GRCh38.p7	8:100279296	TTAGGAGCAAACTAA[C/T]AGCTGGTAGTGTAGG	25897
rs563753029	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100261246	ACTACAGGTGCATGC[C/T]ACCAAATCCGGCTAA	25897
rs563769741	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294644	CTTTCAGCTGCCCTA[C/T]ACTACATAGACTTTT	25897
rs563789326	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310246	GGGCGGCTCTGGACG[C/T]GGCTGTTCCCTTGCG	25897
rs563819161	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302191	AAAATCTAAGTTTAA[A/G]AGGATCATTCAAGTG	25897
rs563924518	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311202	TTACCAATTAGAAAA[C/T]TGAACAAGCTAGGCA	25897
rs563965552	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303824	GTGCCTGTAATCCCA[A/G]CTACTGGCAGGCTGA	25897
rs563985404	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100295259	CCATAACTGAAACTA[A/G]TATTTATCAAAATCC	25897
rs564013818	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271680	CAATGTATTTTTGAT[A/G]GGTCTCTATATACTT	25897
rs564031978	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317580	TCCCATTTGCCTACT[A/C]CAGTCTTTCTTGGTT	25897
rs564052576	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100262329	TGCATGTACGTACAT[C/G]TCTGTGAGCCATTTT	25897
rs564053484	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304503	TCCCACCCCCACTTA[C/T]GCACTCACATTACTT	25897
rs564092200	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305082	CTGGCATGACAGGTG[C/G]CTGCCACCAAGCCCA	25897
rs564188815	in-del	-/CAGTAAAC	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100321902	GTGGCTTAAAATATT[-/CAGTAAAC]CATGCTGTGAACAGA	25897
rs564273920	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100296117	TTTTTTCCTTTTTTT[C/T]TTTTTTGAGACGGAG	25897
rs564280683	snp	G/T	0.00398564	0.0444627	intron-variant	RNF19A	GRCh38.p7	8:100333683	CAATAGCTGGGCATG[G/T]TGGTGTCTCCTGTAG	25897
rs564299773	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318393	CTTCACTGCCTTCAG[A/C]TTGAATTTTTCTCGT	25897
rs564317723	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326061	TGTCTAAAGCCTTCA[A/G]AAGTGCCTGTAATCT	25897
rs564318459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263253	GAGACGGACTGGCCA[A/G]GAAATATGGTAAGAA	25897
rs564361165	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100295505	GGGAAATCCTCAACC[C/T]TAGACTCACTATTTT	25897
rs564363779	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288911	TAAAAATACAAAAAA[A/C]TAGCCGGGTGTGGTG	25897
rs564549518	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279986	TTCTTTTAATTTTTC[A/G]TAACTTCAATCTCTT	25897
rs564580645	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289382	AATAAAATCAACAGA[C/G]AGTATTAAGGGTATG	25897
rs564625155	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100264570	TACTGCAGGCTCAAT[C/T]TAAATTGTCCTCAAA	25897
rs564670658	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282009	ATTCTGGTTCTTTTT[C/T]CCACTATATGCTGCA	25897
rs564716992	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100281945	TAGACAAAGGGAGGT[C/T]CATCTCCTGGTTCCC	25897
rs564746162	in-del	-/TTGGCC	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100278183	AAATAATCTTTGGCT[-/TTGGCC]TTGGCCTTGGCCTTT	25897
rs564770874	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312649	AGAAAGAAAACCGGG[C/T]GCAGTGGCTCACGCC	25897
rs564776312	snp	A/G	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100259798	TTTGTCTAATGATAG[A/G]AATTATTCCTTTAAT	25897
rs564802219	snp	C/G	0.0119091	0.0762411	intron-variant	RNF19A	GRCh38.p7	8:100319795	TCAGCCTCCCAAAGT[C/G]CTGGGATTACAGGCG	25897
rs564837190	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100265280	TGAATAAACAGTATT[A/T]TTTTTTTCTCAGATC	25897
rs564884979	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100313283	TAATGAAAAGGAAAT[A/T]CACTTACCAGAGTAA	25897
rs564903963	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100305620	CAACACTGCTGAAGA[A/G]ATAGTTATAAAATAA	25897
rs564985954	snp	A/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100306487	ATGGCATAGCTTTTT[A/T]AAAAAGTTATCAATA	25897
rs564990295	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297800	TATCTATCTTACTCA[A/C]CTTAAAGCTGGAAAA	25897
rs565018993	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100330150	CATCCCTTCCACTTC[C/T]TCCAGAGTTTGCTCC	25897
rs565034848	snp	A/G	0.00597247	0.0543191	intron-variant	RNF19A	GRCh38.p7	8:100267543	CCCAGATAATTTTTA[A/G]ATTTTTTTGAGAGAT	25897
rs565075375	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100268358	AGTAATCCAAAAAAA[A/C]AGCTTTGAACTACAG	25897
rs565098544	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100284137	TAATAAGTAAGAGCA[A/G]TGACAAGCTTACTGT	25897
rs565166952	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100308477	TTAACTCAATTCAGA[C/T]AGTTCAGTCAGTGTT	25897
rs565217850	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100327554	CTGTGCCTGGCCACA[A/G]TTACTTCTTATATGC	25897
rs565255838	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301268	ATGTGACTTACCCAC[A/G]CAGCTAACGTGGCAG	25897
rs565321520	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328729	CCCCCATCAGCCTCC[C/T]AAAGTGCTGGCATTA	25897
rs565381112	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314918	AGCTTAGCTATGCAC[A/G]TGACATGCCTTCCCT	25897
rs565415348	snp	A/G	1.65061e-05	0.00287277	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259186	ACTGCTTCCACTGTT[A/G]TGCCTGAATTTGGAT	25897
rs565447144	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100322183	TATGAAGTCCAAATG[A/G]CATCTTCTTCCTATA	25897
rs565459290	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100319945	GGTTCAAGCAATTCT[C/G]CTCCCTCAGCCTCCC	25897
rs565495004	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100284473	TCCTCTGTCCTTTGT[A/G]GGTAAGACTATGACA	25897
rs565764647	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276360	CTGTATGATTCCATT[C/T]ATATATTTTTGAAAT	25897
rs565764779	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267821	CTGGGATTACAGGCA[A/C]CTGCCACCATGCCTG	25897
rs565769638	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100308813	GCCAACATCTAGGTT[G/T]GAAAATTGCAACGGC	25897
rs565805464	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100333729	AGGCTGAGGTGGGAG[G/T]ATCACTTGAGCCCAG	25897
rs565864734	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100287311	ATGTAACGCAGAGAC[A/G]ATATAGAAATGAGTA	25897
rs565954124	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100314583	CCCCCCATCCTTTCC[C/T]GTCTTCCTTCTCTTC	25897
rs565977505	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270350	CCTGGTCCCATAGAA[C/G]TCTTCTGAATGGTAG	25897
rs565986779	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309483	GTCTCCCCCGCTTTA[A/G]GGGCAGGAGACAGCT	25897
rs565994424	in-del	-/TCC	0.0111196	0.0737302	intron-variant	RNF19A	GRCh38.p7	8:100324823	TCTTCCTTCCTTCCT[-/TCC]TTCCTCCTTCTTCCT	25897
rs566000507	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301451	TCCTGTGGCATTAAA[A/C]GCCCTCCACAGTGCA	25897
rs566014689	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100271130	AATTCAGGTTTCCTT[A/G]GCACTTCTTCTAGGA	25897
rs566036265	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293189	GCCACACACTGTGGC[C/T]CAAGGGTTGGGGAGC	25897
rs566038243	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302336	GTTTTGAAGGTAAAA[C/G]TGTAAGGATTTCCTG	25897
rs566100698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100261827	TTAAATTCCTCCATG[A/G]TTTCAGAGAGGACAT	25897
rs566163430	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303284	TCGGCTTGCGGTTAC[A/G]TCACTCCAATCTCCG	25897
rs566202307	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100322218	TCTGTTTAGTCTATA[C/T]TGAAAATCTGTTGTT	25897
rs566226143	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330144	AAACACCATCCCTTC[C/T]ACTTCTTCCAGAGTT	25897
rs566245149	in-del	-/GTTC	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303717	CACTTGAGTCCAGGA[-/GTTC]GTTCGAAATCAGCCT	25897
rs566290512	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100295598	TGTCTTTGTGCAGCA[A/T]TTACTATATGTAGTG	25897
rs566305997	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278281	ATGACCATTTGATCA[C/T]ACAAGTGACTATCAT	25897
rs566325814	snp	A/C	0.00953873	0.0683987	intron-variant	RNF19A	GRCh38.p7	8:100276172	AAAGCAGCCTTATTC[A/C]GAATAACCAAAACTG	25897
rs566343866	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310616	AGGAAATGTCCTTTC[C/T]CAGAGGACGGCAGCA	25897
rs566376038	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100296294	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	25897
rs566499077	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311080	TAACTAAATATATCA[C/T]TCTCCCAGTCCTTGT	25897
rs566594262	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288238	ATTCTTGAAAAGTTC[A/G]ATTTACAGAAGACTG	25897
rs566597701	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100326240	GCTTTTTCTGTTCTT[A/T]CTTCTGAACTTCAGA	25897
rs566636013	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319305	TTCTTAGGATGAAAG[C/T]TTTTTTCTTTTTTAA	25897
rs566636976	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100279561	GTACTTTTATTTTTT[A/G]TTTACTTTTGAGATG	25897
rs566759301	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100300417	CCAGCGCTTTGGGAG[A/G]ACAAGGCAGGCAGAT	25897
rs566804351	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100333269	CCTTGGACTTCCCAG[A/G]TCCAGAACAATGAGC	25897
rs566964550	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100263918	ACTTCTGAATGAATA[C/T]TATTAGGCCTAGTAA	25897
rs566964611	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100273213	AAATGAAGTTTTTTT[A/T]TAAAACAATCGCCTT	25897
rs567040389	snp	C/T	1.65737e-05	0.00287864	intron-variant	RNF19A	GRCh38.p7	8:100264631	AAAACTTTAACTCCA[C/T]AAAATTGTAGGTAAT	25897
rs567071386	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100305781	GCATTAGCTCCTATA[C/T]TTCTGCACATTTCAC	25897
rs567128545	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100265955	ATTCCTGCTCCTCCC[C/G]ACTCCCATTCCTGGG	25897
rs567191926	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297385	TCTGTATCATCTGTA[A/G]AATGGGGAAAATACT	25897
rs567216225	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100266945	TTTCTGATTATAAAA[C/T]GTATGTTGAATATAA	25897
rs567224023	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328137	CCACCCACTCCTCAC[A/G]CAATGCACCTCCCTT	25897
rs567230670	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289690	TCTCTTACACTACTC[A/G]TGGGAGTGTAAAATG	25897
rs567250945	snp	C/T	1.64811e-05	0.00287059	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258668	TTAGGTTTTATTCCA[C/T]TGTTACCATGTTCTT	25897
rs567257184	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285852	ATGAAGCACCTCTTG[C/T]ACCCTGGGGTTCTAT	25897
rs567295098	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335527	TGAGTACATATTAAA[A/T]ACTTTTTACTATTTT	25897
rs567311737	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334677	CTTGTTGATTCTAAC[A/G]GTTTCATTGAGTCCC	25897
rs567316743	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100290464	TCACTTTGTGATACA[C/T]ACACGACCCAGAAAC	25897
rs567333410	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100327737	GAAAACATCCGGTTC[C/T]TCTTTTGAAAATAAC	25897
rs567339265	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100259303	TCTTTTTGTTCAGAT[C/G]ACTGGGGGAAGGGTT	25897
rs567359588	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100299687	TTGCTTGAACCCAGG[A/T]GGTGGAGGTTGAGTA	25897
rs567411240	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100332002	ATATATTAACTAAAT[-/A]ATTTCCTATTGGTAT	25897
rs567412422	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326990	GGATCTGGTCTAAAC[A/G]TTCTGATTAACAGTT	25897
rs567421858	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274462	GTTACAAAAGTATTA[A/C]ATGTCGAACATTCTG	25897
rs567452963	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320049	CCATGTTGGCCAGGC[C/T]GGTCTCGAACTCCTG	25897
rs567478994	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100275820	AATGTAGTGACTATA[-/G]GTTAGTTTTAACTGT	25897
rs567529990	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100325420	CTAATTTGCCCCTCT[A/G]TTTAACCTGGCCAGT	25897
rs567573817	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100314413	ATTTGCTGAAAGTTA[C/T]GTAGCTAAGTGGCAG	25897
rs567590134	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307788	AAATTTGGGAAGTGC[A/G]TTTACTTTCCACCAA	25897
rs567658195	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315048	AGTGTGCTGGCACAT[A/G]CCTGTAATCCCAGCA	25897
rs567798449	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100301060	ACTGAATTTAGAGCT[A/C]GTAGGTTCGATGTAT	25897
rs567823869	snp	C/G/T	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100316374	TTGCCACTGCTGTCC[C/G/T]GGGCAGCCTGCTTTT	25897
rs567832622	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337180	TGAGGAATCAAAACA[C/T]ACTGGAGCCAGCACA	25897
rs567840826	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100286848	TCTGACAACTGTACA[-/C]AATAAATACTCTATA	25897
rs567871807	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100276287	TGCAAGTAACACCTT[A/C]GGTGACTCTTCAGAG	25897
rs567910346	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100302147	GTGAGACAGGGAAAC[C/T]TGGGTTTCTAAAGTG	25897
rs567929134	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276438	GGGGAAAGAGTGGGG[C/G]GAAGTACATGTGATT	25897
rs568128639	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100285485	GCTAGTATTAACTAT[A/G]TATTATGATGACATT	25897
rs568138810	snp	C/G	0.000399281	0.0141238	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100270011	ATGGCTTTATATCAT[C/G]AGCTATTGGGAACAC	25897
rs568153882	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100260281	ACTCCATTATTCTCA[A/C]TCAGCATATGGCACT	25897
rs568157468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100309044	TAATGAACCCTAAAC[C/T]TCTTTTTCTTCTTCC	25897
rs568192454	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100260894	GATGTCCTGACTCCA[A/C]CTGTTTCCCAGGACT	25897
rs568276084	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257925	GGCATCAACAATAAA[A/C]AAGATAGAGTACCAG	25897
rs568302067	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100318408	ATTGAATTTTTCTCG[C/T]GCTATATTTTATGTA	25897
rs568318383	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100261899	TTTTCAGGCTAGTCC[A/C]CTAGAAGCAGTGGGA	25897
rs568325932	in-del	-/AGA	0.00318978	0.0398085	intron-variant	RNF19A	GRCh38.p7	8:100273052	TTAAATTTTTTGTAG[-/AGA]AGGAGTCTCGCCACA	25897
rs568367862	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303234	GGAGAATGTGTCCTT[C/T]GACTCTTCCAGCTTC	25897
rs568403328	snp	A/G	3.29739e-05	0.00406028	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287572	AAGCATAAATTCTTC[A/G]TATTTTTCCATCAAG	25897
rs568403839	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100262696	TTAGACATGTGACTA[C/T]GGCTGCACTATGGAC	25897
rs568416582	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100331142	GTGCTGGGCAATTCA[A/T]TAAGAAAGACAACAT	25897
rs568425738	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100286628	GTGGATTTGATTCAG[A/G]TAATGAGTCTTGAAG	25897
rs568503977	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100324288	TTTGGGGTATAGAAA[A/C]AATACTTGAGACTAT	25897
rs568526095	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271362	ACAATTTTAAACATT[C/G]GGGTATGACTAAAAA	25897
rs568528632	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272269	GCTGTCACAATTTAA[A/G]CACATATATAAACAT	25897
rs568542641	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100309670	CTGACCGAGGCCTGA[C/T]CCCCTAAGCCGGCCA	25897
rs568565818	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100267754	CAATCTCAGCTCACC[A/G]CAACCTCCACCTCCC	25897
rs568580621	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100308637	AAAACTCAATGAATC[C/T]AGGTTAAAATAAGAA	25897
rs568584395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100331792	GTATTGATCAAAAGC[A/G]AGTCTGTGCACATAC	25897
rs568620573	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325059	TTACAGGTGCCTACC[A/G]CCACAACCGGCTAAT	25897
rs568641398	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100271919	AAGCCACCGTTCCCC[A/G]ATATGAAAAAGCTTC	25897
rs568671560	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288985	GAATGGCGTGAACCC[A/G]GGAAGTGGAGCTTGC	25897
rs568750968	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304066	GGTTGGAGCAATTCT[C/G]CTGCCTCAGCCTCCC	25897
rs568754593	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100284592	TAGTAACAGAGTCTA[C/G]TAAAGCAAGTGTTTC	25897
rs568761666	snp	C/G	0.00438332	0.0466095	intron-variant	RNF19A	GRCh38.p7	8:100280318	ATAATAAAAAGACTT[C/G]TGAGATTAAAATAAG	25897
rs568761801	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289481	ATCAATAAGAAAACA[C/T]AGACAATCCAATAGA	25897
rs568787711	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100295697	AAATAGATAATTATC[A/G]TAAGCCATCCTTTGA	25897
rs568798558	snp	C/T			missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259238	TGCACCTCCATACTG[C/T]TGCCTTCTCTGAAAT	25897
rs568845700	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100284122	AATACAGATGAAGAA[C/T]AATAAGTAAGAGCAA	25897
rs568866318	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311923	ATTAGAAGGACTTTC[C/T]ATTCTTCACTAGGCC	25897
rs568869324	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304621	AAAAACTGAAAAACA[A/G]ATTTGTTCAGGCAAT	25897
rs568889497	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100298175	GATAGCACAAATGTA[C/T]CTAAATTTACCATGT	25897
rs568900587	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100296367	GCCTCTGCCTCCCCA[A/G]GTGCTGGGATTACAG	25897
rs568956286	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100296385	GCTGGGATTACAGGC[A/G]TAAGCCACCACGACC	25897
rs568972937	snp	A/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100333367	CTAAGACAGCTGTTG[A/T]CTTATAAGTAAATCA	25897
rs568978053	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312775	TAAAAAATACAAAAA[C/T]TGGCTGGGCATGGTG	25897
rs569011603	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100325764	TATGTGTGAGTATGT[A/G]TTACACACACACACA	25897
rs569014597	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100313510	AGGGAGGGGAGTATG[A/C]CGTGGGCCAGGGGAC	25897
rs569087052	snp	G/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100333817	AGTGACACCCTGTCT[G/T]TAAACAATAACAACA	25897
rs569174028	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326281	TTCAATTCTCTTTAA[A/G]TGCATACCACCTAAC	25897
rs569197300	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100273297	TTTCTTTCATAATTA[C/T]CCTCAAAGCTCCTTT	25897
rs569219120	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319928	GCAACCTCTGCCTCC[A/C/T]GGGTTCAAGCAATTC	25897
rs569236539	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334736	GTGCACCCATTCAGC[A/G]CTTTCCTGTCTGGTT	25897
rs569326023	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335632	TGAACACAATTTAAC[C/G]TTTTCTTAAAGACTT	25897
rs569400510	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257482	CTAATCATACATGGA[C/T]CTTTTGTACTTGGTA	25897
rs569400754	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100262137	AGTTCTGTCTACAAG[C/G]TATTATTAAGATCTG	25897
rs569463259	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100298186	TGTACCTAAATTTAC[A/C]ATGTATTGGGTTAAA	25897
rs569464506	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100299310	TAGATGATTACAATT[C/T]TCTAGGATAAACAAA	25897
rs569524998	snp	C/T	0.000115522	0.00759919	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258804	CAGGAAGAATGTTAA[C/T]AGTAGCAAAGCGGGT	25897
rs569538207	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291258	CCTGCCTAACAAACC[C/T]GGCACCGTACTAAAT	25897
rs569691953	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328670	AGAGACGGGGTTTCA[C/T]CATGTTGGTCAGGCT	25897
rs569695541	snp	A/G	0.00398564	0.0444627	intron-variant	RNF19A	GRCh38.p7	8:100330897	ACAGCATTAATGCGA[A/G]AAGTGCAGACTGGCT	25897
rs569706598	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283834	GGTTAAATACTACCT[A/G]TATGCCTATGGTCCT	25897
rs569720443	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275242	ATCCAACTAAAGATT[A/G]TTCCTGAAAAACATT	25897
rs569751675	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267733	CTAGGATGGAGTGCA[A/G]TGGTGCAATCTCAGC	25897
rs569771475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100320713	TTTCTATGTGGATTA[A/G]ATAAAATAATACACG	25897
rs569812571	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100312117	CCATTCTTTTTGTCC[C/G]TTCCAATTCATAACT	25897
rs569829464	snp	G/T	0.00755907	0.0610114	intron-variant	RNF19A	GRCh38.p7	8:100275975	AAATAAAAAAAAACT[G/T]TTTTTTTTTCCTTCG	25897
rs569840165	snp	A/C	0	0	intron-variant	RNF19A	GRCh38.p7	8:100259426	TCTTTATAATGCTTC[A/C]ATGTTTTAAAATAGT	25897
rs569931137	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100302650	AAAAAGTAAATATTA[A/C]AGAGTAGGGAATGAG	25897
rs569947753	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100272021	CATTGTCATATTAAG[-/A]AAAAACAACAGGTTA	25897
rs569964516	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276507	CTGTAATCCCAGCAC[C/T]TTGTGGGGCCGAGGT	25897
rs569976026	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100301351	ATTAATCACCTGGTA[C/T]CCAAATTACCACATT	25897
rs570000683	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277437	CTGCCTCAGACTCCC[A/G]AGTAGCTGGGACTAC	25897
rs570019744	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100328008	GTAAGAGTCTCGCAT[C/T]ATGATGAGTCTGAGA	25897
rs570021600	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100300579	GGTTGCTTGAGCCCA[A/G]GAATTCCAGGCTGCA	25897
rs570050903	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100317302	GGCAGAGGAGGTGCC[A/G]AGAGCAAGCGAGGGC	25897
rs570053825	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100308689	AAGAACCATGTTCTT[C/T]AAAAAAAAAAAATGT	25897
rs570097559	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100319863	TTTTCGAGATGGAAT[C/T]TTGCTCTTGTTGCCC	25897
rs570184031	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100318726	CTTAGATATGACCCA[G/T]AAGCTTGATACCAAA	25897
rs570212665	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310435	TCTCCTCCAAGGACA[A/G]GTCGGGGTGGCTGGA	25897
rs570216860	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100302499	GAGATATCTCTTATA[C/T]CTAGGTGGAGATGTA	25897
rs570328337	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270174	AGCATTTTTTCTTCC[C/T]TTCTAAGAAAACATA	25897
rs570328447	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316505	TATAAAGGTTCTCCA[C/T]GTCCCCATCAGATTA	25897
rs570404344	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100276611	ATTTAAAAAATTAGC[C/T]GGGAGTGGTGGCACA	25897
rs570524756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100332085	TCTGGGTTATATATT[A/G]TTTTACACATATTGT	25897
rs570583290	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294821	ATCTCCACAATATAA[A/C]TGCTTACTAGACTGC	25897
rs570612477	snp	C/T	0.00358779	0.0422022	intron-variant	RNF19A	GRCh38.p7	8:100262322	TGAAAAGTGCATGTA[C/T]GTACATGTCTGTGAG	25897
rs570671136	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100287229	TGGATGAGAAAACCA[A/G]TTTTGTATACAACTA	25897
rs570702411	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100292883	CTAATTGTTACATAT[C/T]TACTTTCTGGTACTT	25897
rs570737913	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100295538	ATCTGCTCAGCCTCT[A/G]GTGCTACATAAACGT	25897
rs570777127	snp	C/T	9.88908e-05	0.00703105	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288068	TCTGAACCCATTTGC[C/T]GATGTAAACTCATGT	25897
rs570808778	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100325115	GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA	25897
rs570811228	in-del	-/CAA	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100287017	AATGCTTATGTATAT[-/CAA]CAACATGAACACATC	25897
rs570897963	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100279409	AGCAGAATCTTACTC[C/T]GTCACCCAGGCTGGA	25897
rs570898627	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100314360	TCAAGAATCCCTAAA[C/G]CTCCCAAATTAGGAT	25897
rs570942723	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100272089	TCTTAGGGTGGTAGC[A/G]GTAAGGGGACAGAGG	25897
rs571001768	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318698	ATTAAATTAATTTTC[A/C]AGCTGGAACACTCTT	25897
rs571030599	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272679	GTAGCTGGCACACAC[C/T]ACTAGAGATGCACAC	25897
rs571077582	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315396	TGTTTGTTTCACTGG[A/C/G]GGGGAAAAATGCAAC	25897
rs571122830	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100312039	GTAGTTTGTTCTTTC[C/G]TCAAAGCATGCTTCT	25897
rs571146765	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100296410	ACGACCAGCCTCCGG[A/G]CATTATTCTTACTGC	25897
rs571165983	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304684	TCAAACCAACCTAGT[C/T]GCCTCTCCTGATTCT	25897
rs571184792	snp	A/C	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289046	CCCTGAGCAACAGTG[A/C]GAGACTCCATCTCAA	25897
rs571255920	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305254	GCAAAGTCATTTTGT[A/G]CGGAGATGTAAAACT	25897
rs571310005	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100290348	CTCAAGTGATCCGCC[C/T]GCCTTGGCCTCCCAA	25897
rs571319296	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100266639	TCCCAGCTTCCTTAA[C/T]AGCGGGGGCTACAGG	25897
rs571334908	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289518	GGCAGGGGACTTAAC[A/G]GGCATTTCACAAAAG	25897
rs571364430	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100301412	TCCACTGGTTTCCCC[A/G]AGATGAAGAATAAAT	25897
rs571373977	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306074	CACTTCTACCAAAGT[C/T]TCTTCAATTGGCAAC	25897
rs571412180	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306874	GTTGGAGAAAAAAAA[A/T]TCCTAAGTAAAGAAA	25897
rs571416048	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100333872	TTTATTTACGACCCC[A/G]TAATGACTCCCTGTT	25897
rs571453385	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100326436	TAGCAAATTCTAACT[A/G]AGAATCAAAAATATG	25897
rs571455214	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100334601	CTTGTGCCCCACCTC[C/T]GAGCTCCAGAATTTT	25897
rs571528022	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100320613	AATGACTATATCAGG[A/G]TGATGAATGCCCATA	25897
rs571529258	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319973	CCCAAGTAGCTGGGA[C/T]TACAGGTGCCCGCCA	25897
rs571540596	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100326826	GTATTTGACTCTCTT[C/T]GATGAAAGAAGTGCT	25897
rs571588086	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19A	GRCh38.p7	8:100265825	GAATCCCATTTCCCA[A/G]CATTGACTAGAGGTT	25897
rs571732401	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100298981	AGGTTTAAAAAAGAT[A/G]CCTAGCTGTCAAAAA	25897
rs571752178	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100314051	CATGCCTGGCTAATT[C/T]TTGTATTTTTTGTAG	25897
rs571766268	snp	G/T	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100294675	CTTTAGGGGGAAAGA[G/T]GTATAAATTTTTTAA	25897
rs571895230	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336375	ATTCCAAAGAAAGGA[C/T]GAGGAAGTCAGTTAG	25897
rs571904690	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100260489	TGCCCAGGCTGGTCT[C/T]AAATTCCTGGCCTCA	25897
rs571925528	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100283953	TTAATTTTTAAAAAG[G/T]GCGGTCCTCTGTGTG	25897
rs572028543	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275432	TTTAGATTCAGGGGG[C/T]ACATGTGCAAGTTTG	25897
rs572028650	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100266336	CTGTAACTGTACCCT[A/G]TGACCTGAACAATGA	25897
rs572069624	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100309884	TTAACTCCTCAGAGC[A/G]GCGGCAGCGCAGGGT	25897
rs572106971	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100334967	ACTAGGGTTAAAATA[A/G]GCTCAGATCTCCCCA	25897
rs572107014	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100306334	GAACACTTCTGTCAT[A/G]TTGAGAGTTTCATGT	25897
rs572115123	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267065	CAGATCTGACTCAAA[C/T]GTAACAATTTTGTAA	25897
rs572150688	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276166	ATGTTCAAAGCAGCC[A/T]TATTCAGAATAACCA	25897
rs572178058	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100307409	ACAGAAAACTACATA[C/T]CTCAACCATCTGTGC	25897
rs572218051	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100302929	TTATAAGATATAATC[A/G]ATTCCTGTTGAGACT	25897
rs572221676	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100285702	TAGTGGCGCAATCAC[A/G]GCTCACTGCAGCCTC	25897
rs572316315	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100284531	GCCAAATTAATCACG[A/G]ACAATTATTTGTTAA	25897
rs572326470	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100284175	GAATTTTGCTAGTAA[C/T]AGCATTAAAGATCTC	25897
rs572388688	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100261076	GAATGTTATTCCTTA[C/G]ACTTAGAAATCTACC	25897
rs572416672	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100301920	TAAAGGAGGTGTTAG[C/G]TATGTGGAAATCTGG	25897
rs572435476	in-del	-/A	0.00795532	0.062565	intron-variant	RNF19A	GRCh38.p7	8:100329361	AGCCATTCATGAGGG[-/A]AAAAAAAAAGACTTG	25897
rs572458960	in-del	-/CT			intron-variant	RNF19A	GRCh38.p7	8:100273815	TGAGATGGAGTCTCA[-/CT]CTGTCATCCAGGCTG	25897
rs572529087	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100321830	GTGACTAGGTGAATT[G/T]TCAGTGAGACATAAT	25897
rs572529863	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316167	TACAGCTCTTAAGAC[A/G]GCGTGTCTGGAGTTG	25897
rs572531177	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329356	TTGGCAGCCATTCAT[C/G]AGGGAAAAAAAAAAG	25897
rs572537764	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100294223	TCTCCTGAAGAGTGA[A/G]GACTTTTATTATACT	25897
rs572622196	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100294870	TAAAAGATTTTCTTG[C/T]ATTATTCAATACCTG	25897
rs572634995	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330742	CCAAAGTAGTCTGAA[C/T]AATATGTTTGTCCTT	25897
rs572672792	snp	A/G	0.0142736	0.0832652	intron-variant	RNF19A	GRCh38.p7	8:100316675	ATAAAGACTCTCCAC[A/G]TCCCCACCAGACTCA	25897
rs572710830	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100310139	TTTCCCCTCCTCCTC[A/C]TCCCACTTCTTCCTC	25897
rs572825583	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100259591	CCATCACCACTACCT[A/G]ACTTCAGAACATTTT	25897
rs572848637	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100317440	AGAGAGTGCCAGGGG[A/G]AAGGAAATTGTTTCT	25897
rs572848700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325261	AAACATGTTTGATAC[C/T]GAAGGCAGAGAACTT	25897
rs572883641	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318241	GGAAACCTAATTGTG[C/G]AACTGACAGTATTTC	25897
rs573038570	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100278810	TTTAAAAAAAAGTAC[C/T]TCTTCTTGACAAGAA	25897
rs573063443	in-del	-/TTG	0.0174175	0.0916809	intron-variant	RNF19A	GRCh38.p7	8:100315649	TTCTTCTTCGTCGTC[-/TTG]TTGTTGTTGTTGTTG	25897
rs573078548	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288885	ATAACACAGTGAAAC[C/G]CTGTCTCTTTTAAAA	25897
rs573153127	snp	G/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100271590	AGGTAACATCCCCAT[G/T]TATTCTTATGGTTCT	25897
rs573165635	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316455	GTCTGTTTTGACAGG[A/G]TGCTGATTGGTGCCT	25897
rs573242728	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272195	GGTTCATTTAAAATT[G/T]AACTCCAAGTGCCTA	25897
rs573258488	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311501	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	25897
rs573279806	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100262929	TTAAGTGAAGGTTTT[C/T]GGCCCAAGCAACAGG	25897
rs573288320	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100292509	TGGCAATTTTCCAAT[A/G]TAGAAATTTCAAAAG	25897
rs573297678	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304429	ATACCCTAAGATAAC[A/G]GGCTTTTCTAAATGG	25897
rs573431889	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100329979	CAAGTAGAGCTTAGA[A/T]GGTCATGTAAGGGAT	25897
rs573468179	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100265017	TTTTACTTTGTGCTT[A/G]AAAGTTCTGAGTAAA	25897
rs573478611	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100305606	GTATTTCTATTGGAC[A/G]ACACTGCTGAAGAGA	25897
rs573480223	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100277667	AGATATGTTCAAACA[C/G]GACTGAATTAAAGGC	25897
rs573509530	in-del	-/TAAG	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100278304	ACTATCATTTCTACA[-/TAAG]TAATATAAATAATGT	25897
rs573510824	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288766	AAAAGTAGTCAAGAA[A/G]AAGTCCCATATAGGC	25897
rs573512657	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100296511	TAGAAAAAAATAAAA[A/G]TGCTTAAAATAACAG	25897
rs573540704	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100280573	AATTTATACAAATTC[C/T]GAAGAAAAACATGTT	25897
rs573549871	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326989	TGGATCTGGTCTAAA[C/T]GTTCTGATTAACAGT	25897
rs573597379	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100280805	GCATTCACACATTTT[A/G]AAAACAGATTGTCAG	25897
rs573602048	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100281435	AAGTCATTTATAATA[G/T]CTCCTGGGAGAATTT	25897
rs573602904	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289164	TTAAAAAAAGAAAAA[C/T]ACTATGTCTACTGGT	25897
rs573621158	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272864	CCTCACTGCATTTCT[A/C]ATTCTTCCTCTTGTT	25897
rs573695894	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100298478	TAGGTGAGTATCAGT[A/T]TCCAACAAGTTCTTT	25897
rs573736123	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100326479	CTGGGCAGAGGGTAT[G/T]ATACTAGAGACAGAA	25897
rs573818443	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100291631	GTATTCTGGAAATGA[A/G]GAAGGCAGGGCAAAA	25897
rs573880858	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100329287	CACACACATTAGGAC[A/G]TTCTATTCTTTTGGA	25897
rs573949670	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100320854	GAGACACACAAATTT[A/G]TGGTTTCCTATTATA	25897
rs574128972	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100274716	AACAGTTTCAGACTA[C/T]CTTTGGCTATCAGTT	25897
rs574148151	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100294792	GGAAATTTTAGCCTA[C/T]TTATGCATCCACGAT	25897
rs574171119	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328180	GGAAGACTCCACCTT[C/T]TGCCACACCCTCAGT	25897
rs574366291	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267247	GTGTAACTGAAGATA[C/T]ATTACATAAACTTTC	25897
rs574448826	snp	C/T	3.29473e-05	0.00405864	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259064	CTTTTTGATTTTTTC[C/T]CTGCTGTTGCTTCTT	25897
rs574450790	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100268003	CTTTTTGAAAATTGC[C/T]ATCCTTTGTTCTGCT	25897
rs574464371	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100285745	TCAAGTTACCTTCCC[A/G]TCTTGGCCTCTCAAA	25897
rs574487028	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100259615	ACATTTTCATGATCC[C/T]AAAAAGGGATCTTGC	25897
rs574510030	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100269205	GATAACTGAAATTCA[A/G]GTTAAAAATTTATCC	25897
rs574537402	snp	C/T	0.00398564	0.0444627	intron-variant	RNF19A	GRCh38.p7	8:100324533	GAGAGTGGAAGTTCC[C/T]TTCATTCTCTCCTCT	25897
rs574617200	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100322226	GTCTATATTGAAAAT[C/G]TGTTGTTTAGTATAG	25897
rs574658160	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100261226	CAGCCTCCCGACCAG[C/G]TGGGACTACAGGTGC	25897
rs574671632	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100329561	CAATGGTCAGGCCTC[A/G]TCTGGAGGCTTATAT	25897
rs574694091	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276971	CAAAATGGCACCACC[A/G]AGACAAACAGTGAGA	25897
rs574704786	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100297363	CCTTTTGTTCAGAAA[A/G]GACCTCTCTGTATCA	25897
rs574721834	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100293223	GTTCTTGTGGATCCA[C/G]TTTTCATCTGGTGTC	25897
rs574777487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100269642	GTATTACATACTTAC[C/T]AGCATTCTAGTTTAA	25897
rs574815557	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100277772	CATCGCAGTCCCAGA[A/T]AAAGAAAAAAGACCC	25897
rs574829882	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100323387	TCAGCACTGAAACAG[G/T]AAGAAGAAAACAGTA	25897
rs574852346	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100270573	GGTATCTTTAGAAAA[A/G]CAGCCTTTTCCCAGT	25897
rs574902215	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100322771	GGCCTAATTTCAAGA[C/T]TGTGTTTCCAAGAAT	25897
rs574942863	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316229	TGGCTCAGGAGTGAA[A/G]CAGCAGACCTTCGCG	25897
rs574970458	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100335690	GGAGGCTAGATGGAG[C/T]CTGATTCTCTGGGGC	25897
rs575008748	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288478	AATCTTAATAAAAGA[G/T]TCTAGATTTGAGCTG	25897
rs575046040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100279635	TTGGCTCGCTGCAAC[A/G]TCCGCCTCCCAGGTT	25897
rs575152124	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310710	CTTAGCCACAATAGC[A/G]AGCCTACGTGAGGGT	25897
rs575191557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100318839	TGTGCTGTTGGAAAC[A/G]AAGAAAGGGAGAGGA	25897
rs575201070	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100286511	TGATACCTGGGAAAA[C/T]TGGGATTTGCACAGG	25897
rs575214837	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312331	CAAGTGTGCTGGGCA[C/T]GGTGGCACACACCTG	25897
rs575240168	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100331538	GCTACTCGGGAGGCT[A/G]AGGCAGGAGGATTGC	25897
rs575308278	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271661	TGAGAATTAATACCA[C/G]AAGCAATGTATTTTT	25897
rs575333152	in-del	-/GTTTATATCCTGCTGCAGCACTTTTCCTTACTGATGTGTAAGACATAG	0.00676609	0.0577691	intron-variant	RNF19A	GRCh38.p7	8:100292355	GTGCACTAGGCACAT[lengthTooLong]TTCTATTTAATAAAG	25897
rs575410078	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100325289	CTTAAGAGCCTGAAG[A/G]GTTTTTGCAGAGAGT	25897
rs575444799	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100272234	AGTAGCTATAAAAAA[A/G]AGCCTCAAGTGGATG	25897
rs575512108	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100275984	AAAACTGTTTTTTTT[C/T]CCTTCGGATTAAAGA	25897
rs575513791	snp	C/T	3.44436e-05	0.00414977	intron-variant	RNF19A	GRCh38.p7	8:100263988	GGCCTCCCCACTACT[C/T]ACACTGTTAATAAGC	25897
rs575525503	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304493	ACTTACCAGTTCCCA[C/T]CCCCACTTACGCACT	25897
rs575568885	in-del	-/TTA	0.00159617	0.0282053	intron-variant	RNF19A	GRCh38.p7	8:100308352	TTAGCATAATTTGGT[-/TTA]TTAAGTCCCAAGACT	25897
rs575656780	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305028	GCAACCTCTACCTCC[C/T]AAGTTCAAGCAATTC	25897
rs575737386	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297503	GCTAAGTGTGGCCAC[A/G]TTATTAGTCCTGGCC	25897
rs575805188	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258065	TATGAAGAAAAAAAA[A/T]GAAATTTATGCCGAT	25897
rs575936866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100280643	AATCTGACAACAAAA[A/G]TTAGAGCAGTTTGTC	25897
rs575964210	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100327049	CTTGAAATGATTCTA[C/T]GTGGATTGTCTTCCA	25897
rs576000787	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100319785	CCCAACTACCTCAGC[C/T]TCCCAAAGTGCTGGG	25897
rs576005276	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100320118	TGGGATTACAGGCGT[A/G]AGCCACTGTGCCTAG	25897
rs576021582	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100281740	TTTAACATACCTTTA[A/T]ATAACTTTCTTTGTT	25897
rs576037573	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100265193	GAATATTCTCTAAAT[A/G]GTAAAAATTGGCTTC	25897
rs576043266	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100266200	AGCTTTTGGGTACTT[A/T]ATTGACTTAGCAGGT	25897
rs576112961	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100259314	AGATGACTGGGGGAA[C/G]GGTTTCTATGTGGAA	25897
rs576151735	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100275659	CACAAAAAAAAGACT[A/G]GAAGGAAAAACACCA	25897
rs576189474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100276099	CTAGGCATTCTTTGG[C/T]ATTTATCCCAAACAA	25897
rs576257063	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280662	GAGCAGTTTGTCTAG[C/T]AGTTTTTTCTCACAC	25897
rs576280750	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100315448	GGGCTTTAGTCTCCA[C/G/T]CATCATTTCACCTGG	25897
rs576284467	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100306402	AACAGTAATTCTTTA[A/G]TAAATGATTTATAAA	25897
rs576289985	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100290991	AGTCCTTAGAGGTCA[A/G]CCTCCTGGGGCACAG	25897
rs576293770	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100306042	CCTCTAACAACTCTG[G/T]CTCCCTCCTTATGGC	25897
rs576470708	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328538	GTGCAGTGGCACAAT[C/G]TCGGCTCCCTGCAAC	25897
rs576484793	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100328863	TAGACTTGTGCAAAG[G/T]GTCTTCTATAAACCA	25897
rs576504759	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100335923	CAAAGCAGCTATCCT[A/G]TAGGTTGGCCGCTTT	25897
rs576507689	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100320934	TCACGTGTAAAAATG[C/T]ATATACCTTAATTTA	25897
rs576540418	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100267401	TAGAGATAGGATCTT[C/G]CTCTATCACCCAGGC	25897
rs576574286	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100269594	TGGGAAAATTAAATG[A/G]AAGTATTTATGGGTC	25897
rs576599902	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336671	CCTTCCCCTAATATT[A/C]TATGTAACTTGAGCT	25897
rs576650832	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100329709	ACTTGGCTAAGAGAG[A/G]AAAGACTAGAGCAGA	25897
rs576652165	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100259758	TCAGAGAACTTAATA[A/G]TTGGTAGCCACTTTT	25897
rs576689459	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100330562	GTTGCCAGAAGCCAA[A/C]ATGTGGAAAGAGTCT	25897
rs576713448	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316011	AGCCGTGGACCCTTG[C/T]GGTGAGTGTTACAGC	25897
rs576831741	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100301651	CAAGGCCCAACTCCT[A/G]TCTTATCTCCACAAT	25897
rs576880414	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF19A	GRCh38.p7	8:100285802	ACGCCCAGTTGTAGA[-/T]TTTTTTTTAAGCTAT	25897
rs576998030	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100286799	TTGTGGCTTTTACTA[C/T]TCCTGAATAGTATAT	25897
rs577028380	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100330930	AAGGCTCTGAGCTGG[C/T]CTTTCTGAAATCTGA	25897
rs577103910	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100285845	GGAATGTATGAAGCA[A/C]CTCTTGCACCCTGGG	25897
rs577112939	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258316	GGCAAACACACAAAA[C/T]ATGCTTTGCTCTTCA	25897
rs577121725	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100270643	ATCAGTACCCAAAAT[A/G]CAAGGAAGGAAGGAA	25897
rs577154101	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100316851	GGGGGAGGCTCAGGC[C/T]GCACAGCAACTCATG	25897
rs577212403	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100261255	GCATGCCACCAAATC[A/C/T]GGCTAATTTTTTATA	25897
rs577334644	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100280449	AGTTCACGGCATGTT[A/G]TATTTACTCAAATGT	25897
rs577338521	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100272368	CTTCAGTGACTGGGG[A/G]AAAAAAACAACTAAT	25897
rs577359460	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100271443	TGCTAATCCTATCTG[C/T]GTAAGCAGCATGTTA	25897
rs577384523	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310259	CGCGGCTGTTCCCTT[A/G]CGCACGTTCGTTCCG	25897
rs577453254	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19A	GRCh38.p7	8:100326450	TGAGAATCAAAAATA[C/T]GCTGTATACTGTGCT	25897
rs577454468	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310754	TCCATTCATCTCTTT[C/T]ATTTCATTTTTTTTT	25897
rs577523576	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305103	ACCAAGCCCAGCAAA[G/T]TTTTGTATTTTTTAG	25897
rs577649120	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100297573	CTGACCTCTAAATCA[C/T]CCCTGAAAAAAACCT	25897
rs577720744	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100263288	TTTCCCATAAGAAAA[A/G]TGAAGTATTTCAAGA	25897
rs577749855	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100334359	AGTGCTGAGCAGAGG[A/G]TAAGGCTCGATAAAC	25897
rs577806760	in-del	-/GT	0.0107246	0.0724382	intron-variant	RNF19A	GRCh38.p7	8:100279871	GGTTTTGCCATGTTA[-/GT]CAGGCTGGTCTCGAA	25897
rs577816049	snp	C/T	3.57041e-05	0.00422502	intron-variant	RNF19A	GRCh38.p7	8:100264232	CATTACAAACAACAA[C/T]AACAAAATAACTCAC	25897
rs577836435	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19A	GRCh38.p7	8:100326663	CCCTTCAAGTTTCTC[C/T]ATCTTATTTCCTTCC	25897
rs577842733	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312449	AAAATTAGCCTGGCA[C/T]GGTGGCCCACGTCTG	25897
rs577868629	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100312865	AGGCAGAGGTTGCAG[C/T]GAGCTGAGATTGTGC	25897
rs578063050	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290184	CAGTGAAGCAATCTC[A/G]GCTCACTGCAGCCTC	25897
rs578090548	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100282045	GGCCTTCAGTTGTTC[C/T]CAGGGCTACATGCCT	25897
rs578098113	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100302283	AGTAATCTATGAGAA[A/G]GATGACGATGGCACA	25897
rs578111808	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100268063	TATTTTTTAAAAAAA[G/T]TTTTAATTTTTTTGA	25897
rs578132729	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100283123	CATTAATTATGTCCC[A/C]GTATAATAAATGTTC	25897
rs578230082	snp	A/G	0.00279162	0.0372561	intron-variant	RNF19A	GRCh38.p7	8:100320314	CAACAACAAAACACT[A/G]TTTTCAAGATCTACC	25897
rs578235684	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19A	GRCh38.p7	8:100273954	CGCCCAGCTAATTTT[C/T]GTATTTTTTTAGTGG	25897
rs745318377	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100308332	CAAATTTTAAAAGTG[G/T]TTTTTTAGCATAATT	25897
rs745384172	snp	C/T	1.64757e-05	0.00287012	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287825	ATGGAAGTTAATCCA[C/T]TGTCAGAAGAGGTAT	25897
rs745397687	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100259794	GTAATTTGTCTAATG[A/T]TAGGAATTATTCCTT	25897
rs745406883	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100296249	AGCTGTGACTACAGG[C/T]ACGTGCCACCATGCC	25897
rs745470152	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280956	AGAAAATTCCAGGAG[C/T]CTCTCTGCTCTGGTA	25897
rs745480352	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100297492	TTCCACTTATGGCTA[A/C]GTGTGGCCACATTAT	25897
rs745481386	in-del	-/AG			intron-variant	RNF19A	GRCh38.p7	8:100277497	TTTTGCATTTTTAGT[-/AG]AGACGGGGTTTCACC	25897
rs745487132	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283031	CAATTTTTTATTGAG[C/T]ATGAGGTTAGCCTGT	25897
rs745495664	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100328343	CAGCAGTGGAAATTA[C/T]CAAATCCAAGAGACA	25897
rs745515977	in-del	-/GGG	1.64757e-05	0.00287012	cds-indel, intron-variant	RNF19A	GRCh38.p7	8:100261721	CCCTCCCCTATGCTT[-/GGG]GGGTTGTGTCTTGCT	25897
rs745522197	in-del	-/GTT	0.000596342	0.0172573	cds-indel, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258607	TGTCTGATGTGAGTG[-/GTT]GTTATTTGTTTCTTT	25897
rs745560606	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100265836	CCAGCATTGACTAGA[-/G]GGTTCCTTGTCAATG	25897
rs745603009	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100302079	TGAGATACATGAGAA[C/T]GCCAGGTTGTGTGGG	25897
rs745620943	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100287153	ATGACCACAAATAAC[A/C]CCCTCATCATAAACA	25897
rs745625992	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100332502	TTTCCTTTATAAATT[A/G]CTCAGTTTCAGGGAA	25897
rs745664613	snp	C/T	1.65072e-05	0.00287286	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258726	CTGAACAGGAAGCAG[C/T]TTGGGTAACCACAGA	25897
rs745681993	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288984	AGAATGGCGTGAACC[C/T]GGGAAGTGGAGCTTG	25897
rs745713974	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100321019	AAGACATAATCTTTT[C/T]GCTGGTGGAGAGTCT	25897
rs745714264	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100333625	TTTCTGTGTGTTGCC[C/T]GGGCAACATAGCAAG	25897
rs745766993	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100296393	TACAGGCGTAAGCCA[C/T]CACGACCAGCCTCCG	25897
rs745775734	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100274456	ATTTATGTTACAAAA[A/G]TATTAAATGTCGAAC	25897
rs745858831	snp	C/T	3.29582e-05	0.00405931	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258879	CTAGGTCAGAACAAC[C/T]AAATTCAGAAAAATG	25897
rs745900095	snp	A/G	1.72133e-05	0.00293366	intron-variant	RNF19A	GRCh38.p7	8:100274945	TAGAAAAAATTAGAC[A/G]TAAATACCTGCTGCT	25897
rs745926494	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100268002	CCTTTTTGAAAATTG[C/T]TATCCTTTGTTCTGC	25897
rs745937428	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100278235	GCTGCTTTGATAACA[C/T]TTCTCATAGTTCTGC	25897
rs745964127	snp	C/T	3.29728e-05	0.00406021	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259965	CCACTTAGACTGTAC[C/T]GTTCTTTCTGTACAT	25897
rs746024822	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100261317	TGCCCAGGCTGGTCT[C/T]GAACTCCTGAGCTCA	25897
rs746097681	snp	C/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337669	CAGGGGTGAAATGAC[C/T]GGCATTTTGACCTGA	25897
rs746133687	snp	C/G	1.66045e-05	0.00288132	intron-variant	RNF19A	GRCh38.p7	8:100261514	GTAGTTACCAGAAAG[C/G]AGAACCAAACCAAAC	25897
rs746154124	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316143	GCTGCAGACCTTCGC[A/G]GTGAGTGTTACAGCT	25897
rs746181960	snp	A/G	3.29598e-05	0.00405941	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288058	AAGATCTCGATCTGA[A/G]CCCATTTGCCGATGT	25897
rs746243902	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100268470	TCATAGACCTGACCT[G/T]ACAAGGATATACCTA	25897
rs746258656	snp	A/C	3.35098e-05	0.00409314	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288136	TACACACAGCCCTTC[A/C]TTATATTTAGAGATA	25897
rs746343247	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304880	TCTGAGTAGCCCAGA[C/G]TGTTTCAAAGGCATA	25897
rs746431008	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291529	TATACATTTATAATA[C/T]CCCACCAATAAACAT	25897
rs746455249	snp	C/T	1.64868e-05	0.00287109	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268832	TCATTGCAGGAATAG[C/T]AATGCCAGCTATTAA	25897
rs746467833	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100297697	AATCTGGATACCTGA[A/G]TACTACACATGGTTC	25897
rs746481923	snp	A/G	0.000115315	0.00759236	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287917	AATTCCATCCACCCC[A/G]CCATTTAGCTCCCTT	25897
rs746488396	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100281773	TTAAAGGTAAGAACA[A/G]AAAGAAAATATAATC	25897
rs746533244	snp	C/T	3.29554e-05	0.00405914	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288010	GGGTGCCTTTTTGAC[C/T]GAAGGCAAGCTCACA	25897
rs746563507	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100284423	TAAGTCAAATATAAA[A/C]TAAAATACACAAAAG	25897
rs746621743	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100285514	TTACCAATCAATCTA[C/G]TACAAGATAATATAC	25897
rs746646661	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100318104	AGGGATTTATAGGAG[C/T]CATGAAACTTGTTGC	25897
rs746707502	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100270835	GCTCCTTGTATAATA[A/G]TATGGTTACAATGCA	25897
rs746709629	snp	A/G	1.65192e-05	0.00287391	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258760	GCTACACTGATGTGG[A/G]GAATTTTCCAGACGG	25897
rs746745456	snp	A/G	4.94597e-05	0.00497266	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264773	CATCCTTGCCTTCAT[A/G]GCGATTGTGAATCTT	25897
rs746825879	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100323522	ATTAACTGCACGTAT[G/T]CTAGCCAAGAAACTC	25897
rs746853924	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100308572	ATTAAGACGGGTAAT[A/G]GCAAAACTGAAAATA	25897
rs746931499	in-del	-/TC			intron-variant	RNF19A	GRCh38.p7	8:100324889	TTTTTTCTTTCTTTC[-/TC]TCTCTCTCTCTTTCT	25897
rs746942147	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310511	CTTGGCAGTTTGCCC[C/G]GCATTATTCATTCCT	25897
rs746958850	snp	C/T	1.65042e-05	0.0028726	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275146	GCTGGCACATCCAAA[C/T]GCTATCACAGCATAT	25897
rs746963993	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100268290	GGTAGTCACTGGTGT[C/T]TGGACTTTCACAAGA	25897
rs747007396	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100261212	TGATCCTCCTACCTC[A/G]GCCTCCCGACCAGCT	25897
rs747058692	snp	C/T	1.65209e-05	0.00287405	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287554	TGCAACAAGCCACCG[C/T]CTAAGCATAAATTCT	25897
rs747098873	snp	C/T	1.64784e-05	0.00287035	missense, intron-variant	RNF19A	GRCh38.p7	8:100261651	CTCGGATGGCTCCTA[C/T]TCGATCCATGTGGCT	25897
rs747099105	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280722	TGTTTCACATTCATA[C/T]GTATTCAATCCTAAC	25897
rs747135019	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100313676	TTGAAAAGGATCACT[C/T]AGGCTGTTCTGTGGA	25897
rs747229007	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100314780	CAACAACCATGCTTA[C/T]CTCTATAATTTTTCT	25897
rs747231212	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100300136	TAAGCAAAATGTGTC[C/T]GTTTCCCTTTGGGTA	25897
rs747237280	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100315299	TCTAATATAAGAGCC[A/C]ATAAAGTACATATGA	25897
rs747269509	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305055	ATTCTCCTGCCTCAG[C/T]CTCCCTAGTAGCTGG	25897
rs747296127	snp	A/T	1.64838e-05	0.00287083	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268839	AGGAATAGCAATGCC[A/T]GCTATTAAAGCGATT	25897
rs747303094	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100296802	ACCTCAGTTAGAAAA[-/T]TAATTCTATTCCATT	25897
rs747420403	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100305637	TAGTTATAAAATAAA[C/T]ACCTTAGATTGTAGA	25897
rs747444634	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100335942	GTTGGCCGCTTTCTA[C/T]ACTATGAACCAACGG	25897
rs747481962	snp	C/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337010	CAGTTGTTATACAAA[C/T]TTAAAAAGTAATAAA	25897
rs747520546	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100328286	CAGTGTTGGGGCTGA[C/G]ACTCATTGAGTCAAA	25897
rs747523812	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100292985	CACAGATGGAGGTGG[A/G]GGGTGGGAGCAAGGA	25897
rs747529397	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293829	ACTGGCAAATTTCTA[C/T]TGATTTATCTTCAAT	25897
rs747610458	snp	G/T	1.64982e-05	0.00287208	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288103	AATGCTTGTTAGAAT[G/T]GAGACAGGGTCAGTG	25897
rs747613113	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258948	TGAGGGATGGAGCCT[C/T]AAATTCACTTGAGTT	25897
rs747652807	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100330964	CCTTGTAACATTTTT[C/G]CAGGGAATCTTCTTT	25897
rs747657675	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100286767	ACTAATAGTATGCTA[C/T]GTATCACATTAATTG	25897
rs747659238	snp	G/T	1.64906e-05	0.00287142	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268822	ATGCCAATAATCATT[G/T]CAGGAATAGCAATGC	25897
rs747697148	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100270888	AGTGTAACATAACTT[G/T]AGGAAAATTATACAA	25897
rs747707033	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100319240	AAAATTTTAGTGATA[C/T]TATGTTTTATATGGT	25897
rs747794787	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100305824	GTGATTATGCATTAG[A/C]ATAACTTAATTTAGG	25897
rs747835025	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100325100	TTTAGTAGAGATGGG[A/G]TTTCACCATGTTGGT	25897
rs747889244	snp	C/T	3.29468e-05	0.00405861	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259066	TTTTGATTTTTTCCC[C/T]GCTGTTGCTTCTTTG	25897
rs747905006	snp	C/T	1.64811e-05	0.00287059	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287581	TTCTTCGTATTTTTC[C/T]ATCAAGACATCATCA	25897
rs747905914	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310606	GCTCTCGGCGAGGAA[A/G]TGTCCTTTCCCAGAG	25897
rs747921349	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100312005	CCTAGAGGCACCTCA[C/G]ATTCAGGCTGTCCAA	25897
rs748043652	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100298731	GCTTTGTGGTTTTAA[C/T]AATACTCATTACAAG	25897
rs748056857	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100262453	AGTATTCCAGACAGA[A/G]AACTGCCAGTTTAAA	25897
rs748089949	in-del	-/TCTGACA	1.64757e-05	0.00287012	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287818	TTGCTGATGGAAGTT[-/TCTGACA]AATCCATTGTCAGAA	25897
rs748105471	snp	G/T	1.64749e-05	0.00287005	synonymous-codon, intron-variant	RNF19A	GRCh38.p7	8:100261685	ACTTGCACTCAAACT[G/T]CCAGTCAGCCCACCA	25897
rs748107583	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100315172	ACACACCTGTAGTCC[A/G]AGCTACTCAGGAGGC	25897
rs748170221	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100274135	CTCAGGATTGCTCAC[A/G]GAGTAAGTAGAGAAT	25897
rs748201823	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100302183	GATAGTTTAAAATCT[A/G]AGTTTAAAAGGATCA	25897
rs748233329	snp	C/G/T	4.95981e-05	0.00497966	intron-variant	RNF19A	GRCh38.p7	8:100261806	TGATTATCAATTTTC[C/G/T]CCTTCTTAAATTCCT	25897
rs748251870	snp	G/T			utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288189	TTCACATTAAGTCAT[G/T]ATGTAAGAATATCCT	25897
rs748252933	in-del	-/TC			intron-variant	RNF19A	GRCh38.p7	8:100324888	TTTTTTTTCTTTCTT[-/TC]TCTCTCTCTCTTTCT	25897
rs748256249	snp	G/T	1.67486e-05	0.00289379	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258592	AACTTTTAATTCCAT[G/T]GTCTGATGTGAGTGG	25897
rs748278328	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100315999	CTTCAAGAATGAAGC[C/T]GTGGACCCTTGCGGT	25897
rs748418733	snp	A/G	1.68363e-05	0.00290136	intron-variant	RNF19A	GRCh38.p7	8:100268968	GGAAAAAATTATAAT[A/G]TAAATAACTGCTGCA	25897
rs748458893	snp	A/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337249	AACCCAACTGAAGAA[A/T]GCATGTGTGATCAGG	25897
rs748470040	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100307038	AGTTTGCCAAATACA[A/G]TGCAATATGCAATGA	25897
rs748471825	snp	A/T	3.30071e-05	0.00406232	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269954	TCATGTGATTGCAGC[A/T]CCCATCATTCATCTT	25897
rs748531419	snp	C/T	2.4268e-05	0.00348331	intron-variant	RNF19A	GRCh38.p7	8:100259822	CTTTAATTTAAAAAA[C/T]ACTTTCAATTTTTTA	25897
rs748548508	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100326234	CTGCTTGCTTTTTCT[A/G]TTCTTTCTTCTGAAC	25897
rs748572759	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293932	TGTACTTTTCAGTTC[C/T]ATAACATCTATTGTT	25897
rs748601789	snp	A/G			intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309338	CTAAGGCCCCAGGCA[A/G]CACGGCTTGCGGGGC	25897
rs748636742	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100327119	TTTGGTTTGGTTTTT[A/C]TGTTTTTAATCTTAG	25897
rs748665873	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100282392	AATGTGATTTTTAAA[A/C]TTCAAAGAACTACCC	25897
rs748719285	snp	G/T	3.29772e-05	0.00406048	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259925	ATTATCACTAACTGT[G/T]CCCAAGCTGACTGTG	25897
rs748726793	snp	C/T	1.65143e-05	0.00287348	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268923	GCTCCAGGGTTTCTT[C/T]CCCCAAAAAGTACAT	25897
rs748747499	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100299531	TTGGGAGACCAAGGT[A/G]GGCAGATCACCTGAG	25897
rs748773619	snp	C/G	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259081	TGCTGTTGCTTCTTT[C/G]GACCACTTGGTGGCA	25897
rs748804070	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100274293	ACCCAATGGCTACTG[C/T]TGACTCTTCAGGGAA	25897
rs748817067	in-del	-/AT			intron-variant	RNF19A	GRCh38.p7	8:100296590	TGTTAATTTGTGAAT[-/AT]ATATATATATTCTAG	25897
rs748830359	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100328013	AGTCTCGCATCATGA[A/T]GAGTCTGAGAACTCA	25897
rs748907282	snp	C/T			missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275054	GCATCACAGGTCTGG[C/T]TGGGGTGCCAAATCT	25897
rs748977329	in-del	-/A	3.6735e-05	0.00428557	intron-variant	RNF19A	GRCh38.p7	8:100287460	ATTTTATCCACAGAG[-/A]AAAAAATTAACTCAA	25897
rs748987311	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100303084	TGAAGACTTTTGACT[A/G]CATAGTAGTTTCCTG	25897
rs748988655	in-del	-/CTT	1.65395e-05	0.00287567	intron-variant	RNF19A	GRCh38.p7	8:100261808	ATTATCAATTTTCTC[-/CTT]CTTAAATTCCTCCAT	25897
rs749005242	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100295788	GCCCAAAGTAAACAG[A/C]GTTTTTATAAATCTG	25897
rs749034037	snp	A/C			utr-variant-5-prime	RNF19A	GRCh38.p7	8:100313348	CTCAAACTAACGTCA[A/C]TTCTTCTGACATTTG	25897
rs749040022	snp	C/T	1.64743e-05	0.00287	missense, intron-variant	RNF19A	GRCh38.p7	8:100261702	CAGTCAGCCCACCAA[C/T]ACTTCCCTCCCCTAT	25897
rs749044247	snp	C/T	1.64768e-05	0.00287021	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287795	CACTCTATGAAGTCT[C/T]CAATTTGTTTGCTGA	25897
rs749052793	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100298779	GTTATTACAAAAAGT[A/T]AGCTGCTGCAGAAAG	25897
rs749054147	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100263675	TCACATTTCTTTGAA[C/T]AACATTGAGTTGAAG	25897
rs749068230	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100299883	CCCACCTCTCCAATT[C/T]TGGAAGCTCATTTGT	25897
rs749098267	snp	C/T	3.44525e-05	0.00415031	intron-variant	RNF19A	GRCh38.p7	8:100263992	TCCCCACTACTTACA[C/T]TGTTAATAAGCACAT	25897
rs749122184	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100331243	GAGAATCCAAGTGGC[C/T]GTCCTTTTGAACCTT	25897
rs749157160	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100287100	TATGAGAAACATGTC[A/G]ACAAAGAGAAAAAAA	25897
rs749172300	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100319409	TTTGTATTATTATTT[A/G]AAACAAGATAAATGA	25897
rs749179097	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100319866	TCGAGATGGAATTTT[C/G]CTCTTGTTGCCCAGG	25897
rs749204845	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100290770	CTAGATGTTATAGTC[C/T]ATTACACACCTAGGG	25897
rs749241840	snp	C/T	0.000232065	0.0107693	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258605	ATTGTCTGATGTGAG[C/T]GGTTGTTATTTGTTT	25897
rs749266492	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100303075	TTGGTTTACTGAAGA[A/C]TTTTGACTGCATAGT	25897
rs749313047	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288799	GGCGCGGTGGCTCAC[G/T]CCTGTAATCCCAGCA	25897
rs749355285	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100290425	TTAATATGTGCAGTA[C/T]GCATAGTGGTTACAA	25897
rs749399368	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304638	TTTGTTCAGGCAATA[C/T]TAAATAGATGAGAGG	25897
rs749402221	snp	C/T	1.65822e-05	0.00287938	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269988	TATATAAGCAGCACA[C/T]CGTGGACATGGCTTT	25897
rs749498939	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100276268	TCAATAAAGAAAGTA[C/T]TGATGCAAGTAACAC	25897
rs749502376	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291448	AAGACAAGAACCTTT[C/T]ACCTTCAGAAGTGCT	25897
rs749502630	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100331665	AACCAGATATACGGC[A/G]CAAAATTTGAAAGGA	25897
rs749511100	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100335824	TCCCTGCGGAGGTGC[A/G]GGCCTAGACAGCAGT	25897
rs749541664	snp	A/G	1.98297e-05	0.00314872	intron-variant	RNF19A	GRCh38.p7	8:100274914	AATAACTAGTGTTTT[A/G]TGTCAAATATTTTAT	25897
rs749584775	snp	G/T	2.04723e-05	0.00319933	intron-variant	RNF19A	GRCh38.p7	8:100259831	AAAAAATACTTTCAA[G/T]TTTTTAACAGTTTTT	25897
rs749615884	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100327164	GTAAAGAAAAATTAT[C/T]CTCATCTTCTGGCTA	25897
rs749656502	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100309655	GTAGGGGACCCGGAG[C/G]TGACCGAGGCCTGAC	25897
rs749713857	snp	A/C/T			intron-variant	RNF19A	GRCh38.p7	8:100328288	GTGTTGGGGCTGAGA[A/C/T]TCATTGAGTCAAAAG	25897
rs749867009	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100323437	AAAATAACTCCTGCT[A/G]GACAGCCTGTTTTTG	25897
rs749916459	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100277438	TGCCTCAGACTCCCG[A/G]GTAGCTGGGACTACA	25897
rs749926309	in-del	-/TG			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290144	TTTTGAGACACAGTC[-/TG]TGTCTGTTGCCCAGG	25897
rs749929098	snp	C/T	1.69963e-05	0.00291511	intron-variant	RNF19A	GRCh38.p7	8:100270034	GGGAACACAGAGAAA[C/T]CTATTAAGTACATAA	25897
rs749958763	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100324730	TAAACAGAACTTCAT[A/G]ACAAGACATTTTAAC	25897
rs749970239	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100291777	ACAGCTTAAAATATG[A/G]AGAAAATCCAGTAAT	25897
rs749982958	snp	A/C/T	3.29822e-05	0.00406082	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259912	CTTTGGTGCTGGCAT[A/C/T]ATCACTAACTGTTCC	25897
rs749987390	in-del	-/CT	1.64803e-05	0.00287052	frameshift-variant, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275089	ACAGTGGTAGCAAAA[-/CT]CTGTTCCACAGCCCT	25897
rs749990143	snp	C/G	1.6501e-05	0.00287232	intron-variant	RNF19A	GRCh38.p7	8:100260006	TTCCAACCTTAAAGG[C/G]GGGTATGAAATCACC	25897
rs750134657	snp	C/T	1.64773e-05	0.00287026	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287993	GAAATTCTTCTTTTT[C/T]TGGGTGCCTTTTTGA	25897
rs750150459	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100298414	GAATATTTTTAATTC[A/G]ACTACTTATAAATGA	25897
rs750236243	snp	C/G	1.64841e-05	0.00287085	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288084	GATGTAAACTCATGT[C/G]TAAAATGCTTGTTAG	25897
rs750261039	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316533	TTAGTTAGATACAGA[A/G]TATCAACACAAAGGT	25897
rs750276869	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100302760	CATGGAGGAATTACA[C/T]TTTAAAGAAGACAAA	25897
rs750343821	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100334332	TTTTCACCCTCTGCT[C/T]TGTTTCCACACAGTG	25897
rs750368550	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100290322	GGTCAGGCTGGCCTC[A/G]AACTCCTGACCTCAA	25897
rs750434823	snp	A/C	0.000169188	0.00919593	intron-variant	RNF19A	GRCh38.p7	8:100268762	GAATAAGATAATGGA[A/C]TAACAAGAAGTATGC	25897
rs750454731	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100290916	TTTCTTTGGCTCTCC[A/G]ATATCCTGCCAGTGC	25897
rs750470001	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100298130	CATATAATCACTTAA[A/G]TATTACCTGTAAGTA	25897
rs750484656	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326560	AGGTAACCCCTCCCC[C/T]TTTCCTGCTTTACTG	25897
rs750503553	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259028	TTTATCTTCATGTTA[C/T]CCTTTTTCCTCAGTT	25897
rs750531492	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100306419	AAATGATTTATAAAA[C/T]AAAATACTAGATAAC	25897
rs750555037	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259108	GGCACTAGATTTACC[C/T]TCAGGCAAGCCACTG	25897
rs750607849	snp	G/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257252	TGCAGCCCATGGCAT[G/T]TTTCTTTTTACCAAA	25897
rs750608628	snp	C/G			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337759	CTCTTCTTTTTTGCT[C/G]TTTATTCAGCACTTA	25897
rs750619398	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100307441	CTGTAGATTAAAAAC[C/G]ACAACAACAACAAAC	25897
rs750702423	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100270432	GTTCTGTACACTATT[C/G]CTTTAGTGAATGAAC	25897
rs750710733	snp	G/T	1.65658e-05	0.00287795	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287547	CAGGATCTGCAACAA[G/T]CCACCGTCTAAGCAT	25897
rs750712620	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100294975	GTATTAATTCATTTA[C/T]TCTTTCAACAAATAT	25897
rs750785361	snp	A/G	1.64798e-05	0.00287047	synonymous-codon, intron-variant	RNF19A	GRCh38.p7	8:100261754	TGCTACTGATGTTGT[A/G]TCTAAATGCAAATAT	25897
rs750799734	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100330251	AGGAAGGGAACAACT[G/T]TCGTTTGATCTTGTT	25897
rs750822636	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100285358	AATTTTCGTAATTCT[A/G]TATGTTGAATAATCA	25897
rs750838487	snp	G/T	1.79162e-05	0.00299295	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258537	GTACAGTGGTAATTA[G/T]TCTGCAGCATTTATG	25897
rs750850751	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100286249	CCCTGCATACGTCCC[A/G]GAGTTTGCTTCTGCC	25897
rs750889328	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100318882	GGGGGAATCAGATTT[A/G]GGAATGCACAGTCCA	25897
rs750897295	in-del	-/AA			intron-variant	RNF19A	GRCh38.p7	8:100268686	ATACCCTTTGTCTAA[-/AA]AAAAAAAAAAAAAAA	25897
rs750973807	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100325511	TAAGTGACCTCTGAA[C/T]AAGACGTTTCAACTT	25897
rs751031314	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100316589	AGATACAGAGCGTCG[A/T]TTGGTGCACTCACAA	25897
rs751078607	snp	A/G	1.65091e-05	0.00287303	intron-variant	RNF19A	GRCh38.p7	8:100260013	CTTAAAGGGGGGTAT[A/G]AAATCACCAAAATTA	25897
rs751097384	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100312909	CCTGGGCAATAGAGC[A/G]AGACTCTGTCTCAAA	25897
rs751101040	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100280160	AAATCTCCATTCAGT[G/T]CCCGGCCCTTGATTG	25897
rs751133750	snp	C/T	1.64942e-05	0.00287173	synonymous-codon, intron-variant	RNF19A	GRCh38.p7	8:100261574	CATGGCACTTCCTGA[C/T]AGACTCCCCGTTATA	25897
rs751142275	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100286474	ATTACATAGAAATCC[C/T]TGGTGGATGGTAAAG	25897
rs751187309	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100299574	AGACCAGCCTGGCCA[A/C]CATGGTGAAACACTG	25897
rs751195541	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100314290	TTGAGTACATATACT[A/G]TATGACAGGCACTAT	25897
rs751267241	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100284849	GAAACATTATCAGCA[A/G]GATGATCATTAACTC	25897
rs751275427	snp	C/G	4.94686e-05	0.00497311	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288095	ATGTCTAAAATGCTT[C/G]TTAGAATTGAGACAG	25897
rs751294518	snp	C/T	4.97541e-05	0.00498744	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268789	ATGCATTTTACCTTG[C/T]GGCCCACATACACAG	25897
rs751345665	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259047	TTTTCCTCAGTTTAC[C/T]ACTTTTTGATTTTTT	25897
rs751377831	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305377	AATCAGTTAGAAAAA[G/T]ACTACAAAAAGACAA	25897
rs751406441	snp	A/C	1.64825e-05	0.00287071	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268891	GTTCCCAGTTGCCAC[A/C]ATATTTTCTTCTTTC	25897
rs751446027	snp	A/G			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336500	CTGAAGTCCTGAGGT[A/G]ACCTTGGATTCCCGA	25897
rs751451811	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259117	TTTACCTTCAGGCAA[A/G]CCACTGGATGAACCG	25897
rs751487121	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100259375	CCTTAACGCAGAACA[C/T]GTTCTACTTAAAAAA	25897
rs751491336	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291906	CTTCTAAAATAAGCA[C/T]GCAATAAAAACAGCA	25897
rs751583879	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100279403	TTTTTAAGCAGAATC[C/T]TACTCCGTCACCCAG	25897
rs751593516	snp	C/T	1.64779e-05	0.00287031	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287696	ATCCTTAAATATTGT[C/T]GTAAGCAATCCACAC	25897
rs751594658	snp	A/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337832	ATCAGCACCTGGAGT[A/T]AGATTATCTAGTCTA	25897
rs751632144	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305104	CCAAGCCCAGCAAAT[G/T]TTTGTATTTTTTAGT	25897
rs751679141	in-del	-/TTTGGGC			intron-variant	RNF19A	GRCh38.p7	8:100262585	GATCATGTGGGGCCT[-/TTTGGGC]TATGATAAGGACTTT	25897
rs751733839	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100281943	TCTAGACAAAGGGAG[A/G]TTCATCTCCTGGTTC	25897
rs751817434	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283772	TTCATAATTTCACAT[C/T]TAGCATTTCTGGAAA	25897
rs751821430	snp	C/G/T			intron-variant	RNF19A	GRCh38.p7	8:100265976	CATTCCTGGGAAACT[C/G/T]AGCACTGAAGAAGAG	25897
rs751862909	snp	C/T	1.64743e-05	0.00287	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287868	TGGAGTTCTTATCAG[C/T]ACACATTTCAGAATG	25897
rs751879372	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100277034	AACTGCATGTGAATC[C/T]ACCATTACCTCTATA	25897
rs751880519	snp	C/T			missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288096	TGTCTAAAATGCTTG[C/T]TAGAATTGAGACAGG	25897
rs751893153	snp	C/G/T	3.42543e-05	0.00413838	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258575	ATTTCAGTCTGAATT[C/G/T]CAACTTTTAATTCCA	25897
rs751894976	snp	C/T	1.65318e-05	0.002875	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264130	AGACTCCACAACCTC[C/T]GCTTCGACAAAGAGA	25897
rs751895502	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100293794	TTCTTTTTTGTAATC[-/T]TTTTTTCTTCGTTCA	25897
rs751946324	snp	C/T	1.64827e-05	0.00287073	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258651	CAAAATATAAATCAA[C/T]ATTAGGTTTTATTCC	25897
rs751952006	in-del	-/AATGCAAATCTG	3.34342e-05	0.00408852	cds-indel, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269876	AAGCTTACCTTAGAT[-/AATGCAAATCTG]AGATTTCTTTCATAC	25897
rs751968472	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100273848	AGGGCAGTGGCACAA[C/T]CTCGGCTCACTGCAA	25897
rs751994115	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100333244	GCCCTCATCAGATGT[A/G]CCCACTCAACCTTGG	25897
rs752009501	in-del	-/ATG			intron-variant	RNF19A	GRCh38.p7	8:100294000	ACATGTTCGGTCATT[-/ATG]ATATTTCCCCCTTTA	25897
rs752043316	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100295104	TAAGCATTGAACAGA[C/T]ACTTCAGATGATATC	25897
rs752049384	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100263062	AGACACTCAAGTGCA[C/G]ATTAAAGAGGAAAGT	25897
rs752136498	in-del	-/A	1.65332e-05	0.00287512	intron-variant	RNF19A	GRCh38.p7	8:100261530	GAACCAAACCAAACC[-/A]AAAACACACACCTGT	25897
rs752159665	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257510	GTACAAGTTCTGCAC[C/T]GTGCTTTGATTTCAT	25897
rs752167798	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100292628	TTAAAATCCCTTCAC[A/G]TGTTTTCTACTGGTA	25897
rs752176443	snp	C/T	3.3066e-05	0.00406595	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269904	GATTTCTTTCATACA[C/T]AACCAACAAAACTCA	25897
rs752183798	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100286743	AACCTTACTTATAAT[A/C]TCTGGTTTACTAATA	25897
rs752243895	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100265076	AGTGTAATTATGTAT[C/T]GAGCAAAGAGGAAGA	25897
rs752260816	snp	C/G	2.36885e-05	0.00344147	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288214	TATCCTACTTGGTTC[C/G]TTCAGAGAATTCTTG	25897
rs752296422	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288490	AGATTCTAGATTTGA[A/G]CTGACCAGAAAAAAC	25897
rs752384395	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289850	CTTAACAATGCTCAC[A/G]ATAGCATTAGTAATA	25897
rs752391806	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100333376	CTGTTGTCTTATAAG[G/T]AAATCACAGTGCATC	25897
rs752446682	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100279680	AGGGGCGCATCACCA[G/T]GCTTGGCTAATTTTT	25897
rs752455526	snp	C/T	1.64787e-05	0.00287038	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259139	GATGAACCGCCAGCA[C/T]GACTTCGGGTGGCAC	25897
rs752459767	snp	A/C/G	6.12343e-05	0.00553299	intron-variant	RNF19A	GRCh38.p7	8:100269829	TGTCTTACAATATAA[A/C/G]ATTACATTTACATAT	25897
rs752507606	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100277559	CCTTGTGATCTGCCC[A/G]CCTCAGCCTCCCAAG	25897
rs752519277	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100262288	GAAAAATACAAGAGA[A/G]TAAAGGGGAGGAGAG	25897
rs752566459	snp	G/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337535	ATATGATTTACTCAG[G/T]TTGGGCCAAGTGACT	25897
rs752617963	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100308246	TTCCATGGACACGTA[A/T]AATTTAAACTTCAGT	25897
rs752638942	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100280356	ATATGTAGTGTTTGT[A/G]TGTCTGTGAAGAGAG	25897
rs752650499	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326703	TTGAATTCATTCCCT[C/T]CTTCCCTCTTCCAAG	25897
rs752651485	snp	A/C/G			intron-variant	RNF19A	GRCh38.p7	8:100313081	GCCTTAATTTTTGGC[A/C/G]GTATTCTCTTTTGTT	25897
rs752699877	snp	G/T	1.64743e-05	0.00287	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287879	TCAGTACACATTTCA[G/T]AATGTATACTTTCAA	25897
rs752727980	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100263325	GAGTCTCTACCATGT[C/T]GGATATACTGTTAAG	25897
rs752748785	snp	A/C/G	0.000116436	0.00762936	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264164	TGGAACTACGCCATA[A/C/G]ACATAAGCTAACATA	25897
rs752749789	snp	A/G	8.23947e-05	0.00641799	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287763	TGTCTTTAGAATGCC[A/G]CAAAAGGCACAAAGG	25897
rs752822377	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285203	TGTGTTCAATTTTAA[C/T]ACACAATGTGGCAGT	25897
rs752824694	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100321880	TTCTGAGCAGTAGTT[C/G]TTAACAGTGGCTTAA	25897
rs752831384	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283835	GTTAAATACTACCTA[C/T]ATGCCTATGGTCCTG	25897
rs752854364	snp	C/T	1.64819e-05	0.00287066	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258677	ATTCCATTGTTACCA[C/T]GTTCTTCAGCAATAT	25897
rs752869943	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100335144	ATTATCAACCATTAT[-/A]AAAACTCTACTAATA	25897
rs752960826	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100269719	TAATTCCAAATGACT[A/G]GCATAATAACTTGGT	25897
rs752982689	in-del	-/AC	1.9913e-05	0.00315533	intron-variant	RNF19A	GRCh38.p7	8:100269839	TATAAAATTACATTT[-/AC]ATATAAATAGCTCCT	25897
rs753025478	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100318645	ACATTATTATCTAGC[C/G]AGTGAAATGATTCCA	25897
rs753026013	in-del	-/TGT			intron-variant	RNF19A	GRCh38.p7	8:100292439	GCTATCATATGGGTG[-/TGT]GTGTGTGTGTGTGTG	25897
rs753039296	in-del	-/T	0.000473447	0.0153785	intron-variant	RNF19A	GRCh38.p7	8:100259841	TCAATTTTTTAACAG[-/T]TTTTTTCCTTACTTG	25897
rs753044342	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100275726	AATTTTCTTGTTTAT[A/C]TGTTTATACATTTCT	25897
rs753055354	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100321716	TTAAATAATAAGACT[C/T]GAAAGTTGAAATTAC	25897
rs753074253	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100259552	ACAATTCAGTGATTT[G/T]TAGTTGTGATCAGAG	25897
rs753112289	snp	A/G	1.71569e-05	0.00292885	intron-variant	RNF19A	GRCh38.p7	8:100270046	AAATCTATTAAGTAC[A/G]TAAAACTGGTCTAAA	25897
rs753119228	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100295705	AATTATCATAAGCCA[C/T]CCTTTGATCAGACTA	25897
rs753147057	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100323038	TGAGCACAGGCTGCC[A/G]AAAAATGTTGCCAAT	25897
rs753147086	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307766	CTTTACGACTTCACT[C/T]ACATTCAAATTTGGG	25897
rs753264239	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291838	AGAGCAGTGTACCTA[C/T]GTCTTCTAATTTTAA	25897
rs753283376	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100333488	AGAGGCAAGATTCAA[C/G]ATTGCTTATACAGCG	25897
rs753294693	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290209	AGCCTCCATCTTTTG[G/T]GTTCAAGCAATTCTC	25897
rs753299544	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100260563	GTATGAGCCACTGAG[C/T]CCAACCAACATTTGC	25897
rs753313333	in-del	-/ATCTG			intron-variant	RNF19A	GRCh38.p7	8:100294490	AGGGGACATCTAGAT[-/ATCTG]AAGGGAGTTTACCCA	25897
rs753318233	snp	A/T	1.64803e-05	0.00287052	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275049	GAGCAGCATCACAGG[A/T]CTGGTTGGGGTGCCA	25897
rs753320207	in-del	-/CTCA			intron-variant	RNF19A	GRCh38.p7	8:100267564	TTTGAGAGATGGGGT[-/CTCA]CTATGTTGTCCAGGC	25897
rs753358814	in-del	-/AATT			intron-variant	RNF19A	GRCh38.p7	8:100297146	CTTATGAGGTAAGTC[-/AATT]AATAATCTATTTAAA	25897
rs753393349	snp	G/T	1.84797e-05	0.00303965	intron-variant	RNF19A	GRCh38.p7	8:100269848	ACATTTACATATAAA[G/T]AGCTCCTTCTATAAG	25897
rs753443414	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100275843	TTAACTGTCAGGTAA[C/T]GGCATACTGTGCCAA	25897
rs753446187	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100330386	TTCTTGGTTCATAAT[A/G]TTAAAGTCATGACCT	25897
rs753491081	snp	A/G	1.69037e-05	0.00290716	intron-variant	RNF19A	GRCh38.p7	8:100270025	TCAGCTATTGGGAAC[A/G]CAGAGAAATCTATTA	25897
rs753493241	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100324532	GGAGAGTGGAAGTTC[C/G]TTTCATTCTCTCCTC	25897
rs753499795	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100323222	GGGATATAGGACTCA[A/G]TGGTTTTTATTTGAA	25897
rs753533444	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100259668	TTCTTCCCTTTCCCA[C/G]CCCTTGACAACCACA	25897
rs753547792	snp	C/T	1.7663e-05	0.00297173	intron-variant	RNF19A	GRCh38.p7	8:100259268	TATAAGAGTAACAAA[C/T]ACAAACATAATTGCT	25897
rs753586387	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100309646	CTGGGCCGGGTAGGG[A/G]ACCCGGAGCTGACCG	25897
rs753599442	snp	A/C	1.64936e-05	0.00287168	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259905	GCCATTGCTTTGGTG[A/C]TGGCATTATCACTAA	25897
rs753606482	snp	C/T			missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275009	CGTATAGTTCTCAAA[C/T]GTAAGCTCTGGGCTC	25897
rs753607720	in-del	-/A	7.13407e-05	0.00597204	intron-variant	RNF19A	GRCh38.p7	8:100259275	GTAACAAATACAAAC[-/A]TAATTGCTGACTTCT	25897
rs753631002	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326874	GTTTCTAACTCAGAA[C/T]TGGCAAGGTTTATTT	25897
rs753685445	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100281426	ACTTAAATTAAGTCA[C/T]TTATAATATCTCCTG	25897
rs753768637	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100267315	TCGAGGTTGCTGCAG[A/G]GTTAAAATAAGTAAA	25897
rs753776597	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310582	GGAGAGAAGTGCCGG[A/G]ATGTTGCAGCTCTCG	25897
rs753778582	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100302699	TTAAGATGTAGGGGA[A/G]AAGAGGCGAATCCAG	25897
rs753819107	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100310023	GGAGGGGAGGAGTCC[C/T]GACGGCCGCTTTCCC	25897
rs753883845	snp	C/T	1.69911e-05	0.00291466	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264190	ACATAATAGGAACAC[C/T]GATACCTAAAGAGAA	25897
rs753885850	snp	C/T	4.94287e-05	0.00497111	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287986	GCCTATTGAAATTCT[C/T]CTTTTTTTGGGTGCC	25897
rs753888468	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100322236	AAAATCTGTTGTTTA[A/G]TATAGTCCCTTTTAT	25897
rs753911173	in-del	-/AAAC			intron-variant	RNF19A	GRCh38.p7	8:100324461	TCTTGTTTTTCTTTA[-/AAAC]AAACAATGGATTCCC	25897
rs753937249	snp	A/G	1.64779e-05	0.00287031	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264730	GTTACACCACCTGCT[A/G]TGGCCAAATTCCGTT	25897
rs753969136	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100270119	TCTTAAGATGTAGTT[C/T]GTTAACTTATAGCTT	25897
rs753971658	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100271501	TGCTCAAGTAGTAGG[C/T]ATCTCAACAAGACAG	25897
rs753980589	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285967	GAGTATTTGTTATAA[C/T]GACTCACAAAAAGTT	25897
rs753994017	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100297895	AAATATGGGGTAGTG[A/C]TAGAGTATATTTTGT	25897
rs754033231	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100287050	ACTGTGGCACATGCT[-/A]AGGTAGGTACCTTTC	25897
rs754058722	in-del	-/T	1.65051e-05	0.00287267	intron-variant	RNF19A	GRCh38.p7	8:100259275	TAACAAATACAAACA[-/T]TAATTGCTGACTTCT	25897
rs754174822	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100269807	CCAAATTTAAGACAA[C/G]TTATTTTGTCTTACA	25897
rs754184990	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311103	GTCCTTGTTTAGTGT[A/G]TCTGTGTAATTTAAA	25897
rs754191976	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100260618	CCACTATAACTTAAG[A/G]GTTTGTATTTAAAAG	25897
rs754210909	snp	C/T	1.64795e-05	0.00287045	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275092	GTGGTAGCAAAACTC[C/T]GTTCCACAGCCCTCT	25897
rs754333897	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100314271	ATACTATATATACTT[C/T]TTATTGAGTACATAT	25897
rs754439529	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100298630	AAGCCTCCCAAAAGA[A/G]GTATTTCTTAAACAG	25897
rs754456225	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100314087	AGGTTTTGCCATGTC[A/G]CTCAGGTGGGTCTTG	25897
rs754465320	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285273	TTTTATTTATATAAC[C/T]TACACCTCTGTAATC	25897
rs754519599	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100299651	TTAATCCCAGCTACT[A/C]GGGAAGCTGAGGCAG	25897
rs754536136	snp	A/T	1.64779e-05	0.00287031	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288027	AAGGCAAGCTCACAG[A/T]TGAAGCAGAGGACTG	25897
rs754591056	snp	A/G	8.24559e-05	0.00642037	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288098	TCTAAAATGCTTGTT[A/G]GAATTGAGACAGGGT	25897
rs754637794	in-del	-/TCT			intron-variant	RNF19A	GRCh38.p7	8:100294611	TCAAGCCAGTAAGAC[-/TCT]TGATTTTCTGCTTGA	25897
rs754665833	in-del	-/AAC			intron-variant	RNF19A	GRCh38.p7	8:100312938	ACAAAACAAAACAAC[-/AAC]AACAACAACAAAAAT	25897
rs754675621	in-del	-/A	1.64765e-05	0.00287019	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287786	CACAAAGGGCACTCT[-/A]TGAAGTCTCCAATTT	25897
rs754676669	snp	A/G	1.65699e-05	0.00287831	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268790	TGCATTTTACCTTGC[A/G]GCCCACATACACAGG	25897
rs754705449	snp	A/G	4.94482e-05	0.00497209	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268892	TTCCCAGTTGCCACA[A/G]TATTTTCTTCTTTCG	25897
rs754731924	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259052	CTCAGTTTACCACTT[C/T]TTGATTTTTTCCCTG	25897
rs754758276	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291257	ACCTGCCTAACAAAC[C/T]CGGCACCGTACTAAA	25897
rs754775591	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100292267	AGATTGGGAATCCAC[A/G]AGGAACATTTGCTTT	25897
rs754853420	snp	A/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259120	ACCTTCAGGCAAGCC[A/T]CTGGATGAACCGCCA	25897
rs754868272	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100277812	TAATCAAAGTTTTAA[A/T]CTAAAGTATCTATAA	25897
rs754900513	snp	A/G	1.65081e-05	0.00287293	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287557	AACAAGCCACCGTCT[A/G]AGCATAAATTCTTCG	25897
rs754957173	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100279485	TTCAAGTGATTCTCA[C/T]GCCTCAGCCTCCCAA	25897
rs754961621	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100301722	TACTCCATGCTCTTA[C/T]ATACAAGTTTACAAT	25897
rs755023111	snp	A/G	1.64779e-05	0.00287031	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287719	ATCCACACAAGATCT[A/G]TGATGACAAGTCATT	25897
rs755069200	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100314891	GTGAGAGAAAGAGGA[A/G]GCAGGCACAGAAGCT	25897
rs755096996	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100282250	TGACTCATTAAAACA[A/C]CACCAAAAATCTTAG	25897
rs755132373	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100317757	AGGATGCACTGGGGC[A/G]GGATGTCAGCAGGTG	25897
rs755139629	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100328082	ATGCATTATGGGAGG[C/T]GAGATGAAAGGGCAG	25897
rs755193155	snp	C/T	3.30486e-05	0.00406487	intron-variant	RNF19A	GRCh38.p7	8:100261802	AGTATGATTATCAAT[C/T]TTCTCCTTCTTAAAT	25897
rs755229606	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100315904	CTAGTTTTCCACAAG[C/T]TCTCCAGGTAATTCA	25897
rs755264715	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288260	AGAAGACTGCTATCA[C/T]GGATGTTCTGAAAAA	25897
rs755293164	snp	C/T	1.64803e-05	0.00287052	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258661	ATCAACATTAGGTTT[C/T]ATTCCATTGTTACCA	25897
rs755391019	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100274006	CCCAGGCTGGTCTTG[A/T]ACCCCTGATCTCAAG	25897
rs755449283	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100307634	AAAACAAAAAGTTTG[A/C]TTTTAATTACCCATA	25897
rs755457894	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100321538	TGCATGAGAGTTGGA[A/G]TCAACTTCTTTCAAG	25897
rs755493774	snp	C/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100338041	TGTAGTGCAGTAGCA[C/T]GATCTTGGCTCACTG	25897
rs755526744	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100293878	TGCCATCTCCAATCT[A/G]CTGTTAAATCCATCC	25897
rs755534775	snp	C/G	2.66244e-05	0.00364849	intron-variant	RNF19A	GRCh38.p7	8:100259806	ATGATAGGAATTATT[C/G]CTTTAATTTAAAAAA	25897
rs755561162	snp	A/T	1.71249e-05	0.00292612	intron-variant	RNF19A	GRCh38.p7	8:100270043	GAGAAATCTATTAAG[A/T]ACATAAAACTGGTCT	25897
rs755644586	in-del	-/CTGCAACCTCTGCCTCCTGGGTTCAAGT	1.67091e-05	0.00289038	intron-variant	RNF19A	GRCh38.p7	8:100275174	ATCTTGAAAGAACAA[-/CTGCAACCTCTGCCTCCTGGGTTCAAGT]GAAAAATGATTTAAA	25897
rs755731056	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100321774	GTTGGGTTAACAGGT[A/G]TGAAAACAATATTAA	25897
rs755758616	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289894	TGGAAACAACCCATA[A/G]TTTTATCAACTGTAG	25897
rs755760971	snp	C/T	1.65026e-05	0.00287246	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268917	CTTTCGGCTCCAGGG[C/T]TTCTTCCCCCAAAAA	25897
rs755863515	snp	C/T	3.50207e-05	0.00418439	intron-variant	RNF19A	GRCh38.p7	8:100259261	TCTGAAATATAAGAG[C/T]AACAAATACAAACAT	25897
rs755870561	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100279715	TATCTTTAGTAGACA[C/T]GGGGTTTTGCCATGT	25897
rs755932075	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100313220	AAAAGCCTACATATC[C/G]GTTTGCATGGTGCTT	25897
rs755991997	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100262462	GACAGAGAACTGCCA[A/G]TTTAAAAGCCTAGAA	25897
rs756017759	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100299852	ACTCCATACAAATTA[C/T]TGATAACAGTAGCAT	25897
rs756023849	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100309021	ATTTACTGCCCTTGT[C/T]GCGGGGTTAATGAAC	25897
rs756040893	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100326776	AGTGATACTTATCTT[A/G]AACACTTTAAACAGT	25897
rs756079236	in-del	-/C			intron-variant	RNF19A	GRCh38.p7	8:100312251	CTTATGTCCACGTTG[-/C]ACCCAACAATTAAAT	25897
rs756080424	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283855	CTATGGTCCTGACAC[C/T]GTGGCTAACCATTTT	25897
rs756093230	snp	C/T	3.29544e-05	0.00405908	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287773	ATGCCGCAAAAGGCA[C/T]AAAGGGCACTCTATG	25897
rs756165755	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100267999	TTCCCTTTTTGAAAA[C/T]TGCTATCCTTTGTTC	25897
rs756166044	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100328933	CAGCTAGAGCACGAA[G/T]GGCTTCAGTTCCACT	25897
rs756258022	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100317429	CTGGGCCCTTCAGAG[A/T]GTGCCAGGGGAAAGG	25897
rs756326494	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100269723	TCCAAATGACTAGCA[C/T]AATAACTTGGTTTCT	25897
rs756342854	snp	A/T	1.64936e-05	0.00287168	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258696	CTTCAGCAATATGAT[A/T]CAACTGTGAAACTTC	25897
rs756369704	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100263125	TCGGTCTATGCATTA[A/T]TTAATAGATGAGATT	25897
rs756380034	snp	A/G	1.74781e-05	0.00295614	intron-variant	RNF19A	GRCh38.p7	8:100270063	AAAACTGGTCTAAAA[A/G]TAACTTCTAGCAGTT	25897
rs756411187	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100275807	TTGCCTGTTTAAAAA[C/T]GTAGTGACTATAGGT	25897
rs756411882	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100272760	GTTGCCCAGGCTGTT[-/G]GAAGTTTTAGAACTT	25897
rs756459627	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100333778	AGCTATGATTATGCC[A/G]CTGCACTCCAGCCTG	25897
rs756470350	in-del	-/AATC			intron-variant	RNF19A	GRCh38.p7	8:100263442	AGTGGTAGGGACAAA[-/AATC]AATCTGATTGAGGCC	25897
rs756580644	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100269486	AAGTCAGTTTTTTAA[C/T]AGTAAACTAATGCAA	25897
rs756626923	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100282478	AGGAAGAATAAATTA[A/C]AAATAGCACTCTCAG	25897
rs756631433	in-del	-/TT			intron-variant	RNF19A	GRCh38.p7	8:100291969	AAGAGGACTAAGTCT[-/TT]TTTTTTTTTTTTTTT	25897
rs756643748	snp	C/T	1.648e-05	0.0028705	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275051	GCAGCATCACAGGTC[C/T]GGTTGGGGTGCCAAA	25897
rs756646673	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100328138	CACCCACTCCTCACA[C/T]AATGCACCTCCCTTT	25897
rs756675322	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100297154	GTAAGTCAATTAATA[A/G]TCTATTTAAAGTCTA	25897
rs756679874	snp	A/C	1.64895e-05	0.00287132	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259928	ATCACTAACTGTTCC[A/C]AAGCTGACTGTGCCA	25897
rs756689353	in-del	-/ACAGTTT			frameshift-variant, intron-variant	RNF19A	GRCh38.p7	8:100261549	CACACACCTGTTAAA[-/ACAGTTT]ACAGTTTACCATGGC	25897
rs756721490	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100330652	AATATCCTGATGATA[C/T]TGTTGAGTCTCTGGA	25897
rs756730996	snp	A/G	1.65195e-05	0.00287393	intron-variant	RNF19A	GRCh38.p7	8:100260028	GAAATCACCAAAATT[A/G]TATTTAATATCAGCA	25897
rs756750907	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290251	GGGATTACAGGCATG[C/T]GCCACCATGCTGGCT	25897
rs756758026	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100260789	ATCTATATGGCTATT[A/G]ATAAAAGACTTGGTG	25897
rs756844688	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100275917	CATTTTTCTTCCTAA[A/G]ATGCATGGCAAAAGT	25897
rs756855896	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100277317	ATCCCTTAGTATCAC[A/T]CTCTTTTTTTTTGAG	25897
rs756856000	snp	A/C	5.32042e-05	0.00515745	intron-variant	RNF19A	GRCh38.p7	8:100259271	AAGAGTAACAAATAC[A/C]AACATAATTGCTGAC	25897
rs756859095	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100308213	CTCAAAGACACCTTG[A/C]GATGACATTAAAATA	25897
rs756865777	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100292203	GTTGAGAAGATAATA[A/T]AGAATAAAAAAAACA	25897
rs756874270	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100309660	GGACCCGGAGCTGAC[C/G]GAGGCCTGACCCCCT	25897
rs756878086	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100314414	TTTGCTGAAAGTTAC[A/G]TAGCTAAGTGGCAGA	25897
rs756901379	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100259679	CCCAGCCCTTGACAA[C/G]CACAAATCCACTTTA	25897
rs756983096	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100281489	ATACTATTGATAACA[C/T]CAAGCAAGTAGGGAT	25897
rs756985494	snp	A/G	0.000478173	0.015455	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259907	CATTGCTTTGGTGCT[A/G]GCATTATCACTAACT	25897
rs757014226	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100263826	AGACATTATATTCCA[A/G]TTAGAGGTCAGATAC	25897
rs757025559	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100265822	TCAGAATCCCATTTC[C/T]CAGCATTGACTAGAG	25897
rs757056157	in-del	-/TTTA			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310752	CTTCCATTCATCTCT[-/TTTA]TTTCATTTTTTTTTT	25897
rs757061297	snp	C/T	1.64741e-05	0.00286998	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287898	GTATACTTTCAATAC[C/T]TGCAATTCCATCCAC	25897
rs757066702	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100301849	TGATTACTATTTTAA[A/C]CAGGGTGATCACAGT	25897
rs757156490	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288845	ATGGGCGGATCACAA[G/T]TTCAGGAGATTGACA	25897
rs757183835	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100315667	GTTGTTGTTGTTGTT[C/G]TTGAGACAAGGTCTC	25897
rs757219870	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100270254	AACAATGAGAACAAA[A/G]AATAAAAAAAGAATA	25897
rs757228986	snp	C/T	1.6477e-05	0.00287024	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287988	CTATTGAAATTCTTC[C/T]TTTTTTGGGTGCCTT	25897
rs757255542	snp	A/C	1.72665e-05	0.00293819	intron-variant	RNF19A	GRCh38.p7	8:100264205	CGATACCTAAAGAGA[A/C]ATTAAATCAGTCATT	25897
rs757282274	snp	C/G	4.94336e-05	0.00497135	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264732	TACACCACCTGCTAT[C/G]GCCAAATTCCGTTTG	25897
rs757439095	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100271564	GCATGCAATCTTTGG[A/C]ACAAACTGAAAGGTA	25897
rs757443825	snp	A/G	1.648e-05	0.0028705	stop-gained, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275109	TTCCACAGCCCTCTC[A/G]CCCACAAGTTAATTT	25897
rs757449913	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100267941	CCTCAGCCTTCCAAA[A/G]TGCTAAGATTACAGG	25897
rs757482173	in-del	-/AAAA			intron-variant	RNF19A	GRCh38.p7	8:100268684	AGATACCCTTTGTCT[-/AAAA]AAAAAAAAAAAAAAA	25897
rs757494831	snp	A/G	1.67211e-05	0.00289142	intron-variant	RNF19A	GRCh38.p7	8:100261492	ATTCTCACCTAATTA[A/G]TAATTTGTAGTTACC	25897
rs757496406	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100335842	CCTAGACAGCAGTGC[C/T]CTGGTCTAAGTGGGC	25897
rs757575622	snp	A/G	1.69784e-05	0.00291357	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287511	CTTACCCACAGTCTG[A/G]AGCTGGACACCACCT	25897
rs757588668	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100325113	GGGTTTCACCATGTT[C/G]GTCAGGCTGGTCTCG	25897
rs757593577	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311138	AAACAAACCAAGGAG[C/T]CATGGTCTTTCCGAA	25897
rs757688027	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100270330	TACGTAAAGTTTGTC[G/T]TTGTCCTGGTCCCAT	25897
rs757702229	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100329059	TGACTAATTCCAGGT[A/G]CCTCCAGATCTGTCC	25897
rs757713837	in-del	-/TCTTG			intron-variant	RNF19A	GRCh38.p7	8:100294200	AGAGGCTCTGTAGTC[-/TCTTG]TCTTCTCCTGAAGAG	25897
rs757766178	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100317645	ACACTGTGCTGGTGA[A/C]CTGGACCAGAATCCT	25897
rs757769492	snp	A/G	1.64868e-05	0.00287109	missense, intron-variant	RNF19A	GRCh38.p7	8:100261605	CTGGCTCCAGCTAGT[A/G]CCATGGTGCTGGCCG	25897
rs757818466	snp	C/G	3.29973e-05	0.00406172	stop-gained, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288104	ATGCTTGTTAGAATT[C/G]AGACAGGGTCAGTGT	25897
rs757829297	in-del	-/G	1.68391e-05	0.0029016	intron-variant	RNF19A	GRCh38.p7	8:100270019	ATATCATCAGCTATT[-/G]GGAACACAGAGAAAT	25897
rs757859751	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100277502	CATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	25897
rs757878335	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100324731	AAACAGAACTTCATG[A/G]CAAGACATTTTAACA	25897
rs757949424	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100261016	AAGCAGCTGTAGCAA[C/T]GATTTATAATATAAA	25897
rs757968144	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311290	TATTTTCATTTATGG[G/T]AAGTTTTAAAGCTGT	25897
rs758002255	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100298416	ATATTTTTAATTCAA[C/T]TACTTATAAATGAGG	25897
rs758064708	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311545	AACATAGTGAAACCC[C/T]GTCTCTACTAAAAAT	25897
rs758067678	snp	A/C	4.94572e-05	0.00497254	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288088	TAAACTCATGTCTAA[A/C]ATGCTTGTTAGAATT	25897
rs758208384	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100334344	GCTCTGTTTCCACAC[A/G]GTGCTGAGCAGAGGG	25897
rs758222124	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100302821	TCATTCCCCTCCCCC[A/G]TGTCAACTACATCTT	25897
rs758312300	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304182	GGCCAGGCTGGTCTC[A/G]AACTCCTAACCTCAG	25897
rs758358490	in-del	-/C			intron-variant	RNF19A	GRCh38.p7	8:100259742	TCACTGTTTCCTTTT[-/C]TCAGAGAACTTAATA	25897
rs758359684	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100306539	ATGACAGTGATAAAG[A/G]GAGCAATGCAAGCAA	25897
rs758387650	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100335360	CTATGAGGAAATTGA[A/G]GCACTGTATTACAAA	25897
rs758400507	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100291065	AACAAAAAACATCCA[A/G]TATTGTATGTATAAA	25897
rs758462264	snp	C/G	1.64743e-05	0.00287	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259030	TATCTTCATGTTACC[C/G]TTTTTCCTCAGTTTA	25897
rs758581558	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257334	ATAGAACATTTTAAC[C/T]GCTATCATTGAGGTT	25897
rs758585410	snp	A/C	1.65608e-05	0.00287752	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287548	AGGATCTGCAACAAG[A/C]CACCGTCTAAGCATA	25897
rs758585966	snp	C/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337771	GCTCTTTATTCAGCA[C/T]TTAAAGTCCTACTAA	25897
rs758642585	snp	A/G	1.64849e-05	0.00287092	missense, intron-variant	RNF19A	GRCh38.p7	8:100261620	GCCATGGTGCTGGCC[A/G]TTTCACTCAGGTTGT	25897
rs758652577	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100273546	TCCCATGGTGACTAC[A/G]TTGAGGAAGACCAAT	25897
rs758697529	snp	G/T	0.000148359	0.00861149	intron-variant	RNF19A	GRCh38.p7	8:100261769	GTCTAAATGCAAATA[G/T]TCCAAAGAAACTAAG	25897
rs758751976	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100299472	ATTAGAAGTATTAAG[G/T]GTTTGGACCGGGTGC	25897
rs758767662	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100316822	GCTGCCGTGGAGCAG[C/G]GGGTGGTGCTCCTGG	25897
rs758802239	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100330276	CTTGTTTTTGACCAT[A/T]GTGGACTGTTATTAT	25897
rs758828836	in-del	-/CC			intron-variant	RNF19A	GRCh38.p7	8:100324824	CTTCCTTCCTTCCTT[-/CC]TTCCTCCTTCTTCCT	25897
rs758849738	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100286391	TCAAATCTAATAATG[A/T]ATAATATCTGAATCC	25897
rs758853823	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100318905	ACAGTCCAGATGATA[A/G]CAGTGACCCACAAGA	25897
rs758901002	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100314566	CTAGCAGTACCACAA[A/C]TCCCCCCATCCTTTC	25897
rs758913565	in-del	-/G	3.29992e-05	0.00406184	intron-variant	RNF19A	GRCh38.p7	8:100260003	ACTTCCAACCTTAAA[-/G]GGGGGGTATGAAATC	25897
rs758924992	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326679	ATCTTATTTCCTTCC[C/T]ATGAGCTCTTGAATT	25897
rs758932752	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100283545	CCGTCCTTCAAACAA[-/G]TATGATCAGTCCTAG	25897
rs758935043	snp	C/G	1.79114e-05	0.00299255	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258539	ACAGTGGTAATTATT[C/G]TGCAGCATTTATGGG	25897
rs758947532	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100305551	TTTACTTCTTTAATG[G/T]GGCACTAGAAAATTT	25897
rs758966117	snp	A/G	1.65274e-05	0.00287462	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268929	GGGTTTCTTCCCCCA[A/G]AAAGTACATCCTGAT	25897
rs758970963	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100271911	AATCAATTAAGCCAC[C/T]GTTCCCCGATATGAA	25897
rs759047837	snp	A/G	3.29538e-05	0.00405904	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287620	CAAGCGAATATCATG[A/G]GGATTAAACCGTTCA	25897
rs759058701	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100280174	TGCCCGGCCCTTGAT[A/T]GCTAGTTTTTAAAAA	25897
rs759075285	snp	C/T	3.29913e-05	0.00406135	synonymous-codon, intron-variant	RNF19A	GRCh38.p7	8:100261583	TCCTGACAGACTCCC[C/T]GTTATACTGGCTCCA	25897
rs759076812	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100306656	GTACACAAGTTTTAA[-/A]CACCCAAAGTGATTT	25897
rs759131189	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100327480	TGGTCTCAAACTCCC[A/G]ACTCAAGTGATGTTC	25897
rs759146372	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316103	CTTTCTGGTGGGTTC[A/G]TGGTCTCGCTGGCTC	25897
rs759171950	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100300694	AAAAAATAAAAAAAC[A/G]AAAGCAACATAATCA	25897
rs759200203	in-del	-/AACTGAA			intron-variant	RNF19A	GRCh38.p7	8:100267236	TGCTTCTTTGTGTGT[-/AACTGAA]GATATATTACATAAA	25897
rs759201515	snp	A/G			downstream-variant-500B	RNF19A	GRCh38.p7	8:100256667	ATCTAATGTTGCTAG[A/G]ATAGAATCTCTTAAA	25897
rs759212438	snp	C/G	2.18586e-05	0.00330588	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288202	ATGATGTAAGAATAT[C/G]CTACTTGGTTCCTTC	25897
rs759327903	snp	A/G	1.80117e-05	0.00300092	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258518	ACCAGCTCCAAACAC[A/G]GTTGTACAGTGGTAA	25897
rs759388057	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100307178	ACCAGCCTGCATTTG[A/G]CAGTCAGTTTTCACT	25897
rs759451760	snp	A/G			downstream-variant-500B	RNF19A	GRCh38.p7	8:100256865	AGTATCTTTTTTTCT[A/G]GTGGAAAGGCAGGAA	25897
rs759459756	snp	C/T	3.29788e-05	0.00406058	intron-variant	RNF19A	GRCh38.p7	8:100269818	ACAAGTTATTTTGTC[C/T]TACAATATAAAATTA	25897
rs759482286	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100262178	GTTCCAATTTTACAG[C/T]ACCTCTCACACATTT	25897
rs759483968	snp	C/T	1.65658e-05	0.00287795	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259862	TCCTTACTTGTCCAA[C/T]GGGATGTAGGAATTC	25897
rs759511339	snp	A/G	1.66538e-05	0.00288559	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269999	CACATCGTGGACATG[A/G]CTTTATATCATCAGC	25897
rs759511986	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293356	CACCTTCACGTTTTA[C/T]GGATATTTTTGCTGA	25897
rs759550640	snp	A/C/G			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337472	AGTCTTCATGACCTC[A/C/G]CATCATCAGTGTCAA	25897
rs759566661	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100329550	ACTGAACTCAGCAAT[G/T]GTCAGGCCTCATCTG	25897
rs759631191	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100283082	ACTTTTCTGGAGGAT[A/C]CTTGGGAGGCTCAGA	25897
rs759652548	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100324082	CAATTACTACAGAGC[C/T]GTGATTTTGAGATGA	25897
rs759670033	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100297900	TGGGGTAGTGATAGA[A/G]TATATTTTGTTGAGT	25897
rs759706335	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100296848	GAAGGTGCAACTCTT[C/T]CCACAAGAGTTAAGT	25897
rs759731416	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100332187	TATCTGATTTGGTTT[C/G]GCTCTGTGTCCCCAT	25897
rs759741679	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310718	CAATAGCAAGCCTAC[G/T]TGAGGGTTTGGAGAG	25897
rs759759242	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100321798	ATATTAATCTCCTTA[A/T]ACATCAGAGTTCTTG	25897
rs759796710	in-del	-/AATT	1.65021e-05	0.00287241	intron-variant	RNF19A	GRCh38.p7	8:100264790	CGATTGTGAATCTTG[-/AATT]AATAAAAATAGGGGT	25897
rs759827472	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100302420	ACTGAAATGGGGAAG[A/G]CTATGAAACACAAGT	25897
rs759829810	snp	C/T	1.64985e-05	0.0028721	splice-acceptor-variant	RNF19A	GRCh38.p7	8:100264786	ATAGCGATTGTGAAT[C/T]TTGAATTAATAAAAA	25897
rs759847173	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100310037	CCGACGGCCGCTTTC[C/T]CGAACTCCTCCTCCG	25897
rs759855210	snp	C/T	3.295e-05	0.00405881	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287960	TTATCTTTTTTCCTC[C/T]GAAACAGGGAGCCTA	25897
rs759855290	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100287200	CTGTTATTCCAAAAT[A/G]AAAATTCTCCAAATG	25897
rs759886506	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100333979	CCAAGTGTATTTACT[A/T]CTACTGCCCAATAAA	25897
rs759892328	in-del	-/CTT	3.62398e-05	0.00425659	intron-variant	RNF19A	GRCh38.p7	8:100259286	AAACATAATTGCTGA[-/CTT]CTTTTTGTTCAGATG	25897
rs759955720	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100333293	AATGAGCCAAATACA[A/C]TTCTATTGTTTAACA	25897
rs760005660	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100290515	TCTATGTGTTTTTTT[C/T]CTCCTATGGCTGACC	25897
rs760015711	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100259427	CTTTATAATGCTTCA[A/G]TGTTTTAAAATAGTG	25897
rs760046199	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283364	TCTCCTCCTTGCACA[C/T]TGGGATCCCTCCCCC	25897
rs760064459	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100315501	TTGTCCAGGGAGAAA[A/G]AGATTCTCTTTCAGC	25897
rs760135683	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100322845	GTGGAGTAGTCAGAA[C/T]ACACACACACATTTA	25897
rs760138064	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100267110	TTTACAACAGAATGG[A/C]TTGCTTCATGAGTTG	25897
rs760143416	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100276529	GGCCGAGGTGGGCAG[A/G]TCACTTGAGGTCAGG	25897
rs760152291	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100302562	TAGGAAAAAAGTAAA[C/G]CCTAGAGATGTAAAT	25897
rs760194203	snp	A/C	1.65132e-05	0.00287339	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264067	CACCAACATTTATAT[A/C]ATTTTCATCATCAAA	25897
rs760211371	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100328401	TGTCAACATGCACAG[A/G]TTCTAGTCTAAGGGG	25897
rs760245590	snp	C/G	1.64944e-05	0.00287175	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258629	TTTGTTTCTTTTAGT[C/G]CATCGCCAAAATATA	25897
rs760271900	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316256	CGCGGTGAGTGTTAC[A/G]GCTCATAAAAGCAGC	25897
rs760362145	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303360	CTGTAATGGGTCTAC[C/T]TGTCCCTTACAAAGA	25897
rs760422502	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307367	GTTATCACAAATATT[C/T]TGCCTTCTTTTCCCT	25897
rs760422781	snp	A/G	1.68749e-05	0.00290468	intron-variant	RNF19A	GRCh38.p7	8:100270020	TATCATCAGCTATTG[A/G]GAACACAGAGAAATC	25897
rs760464370	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100332247	TAATCCCCAAGTGTC[C/G]AGGGAGGGATGTGGT	25897
rs760465966	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100276724	TCACACCACTGTACC[-/A]AAAAAAAAAAAAAAA	25897
rs760475877	snp	C/G	1.65083e-05	0.00287296	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259884	TAGGAATTCAGAATG[C/G]ATCCTGCCATTGCTT	25897
rs760528085	snp	A/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337559	AGTGACTGCCCCTAG[A/T]CAAATTAGCTGGTCA	25897
rs760533296	in-del	-/AAG			intron-variant	RNF19A	GRCh38.p7	8:100329764	AGGATCGTCTGATGA[-/AAG]AAGAAGTAGCTTCAT	25897
rs760634948	in-del	-/TTTGT	1.76593e-05	0.00297142	intron-variant	RNF19A	GRCh38.p7	8:100259267	TATAAGAGTAACAAA[-/TTTGT]TACAAACATAATTGC	25897
rs760645680	snp	C/T	1.64914e-05	0.00287149	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259994	ATCTGCTTGTACTTC[C/T]AACCTTAAAGGGGGG	25897
rs760658220	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100281218	GAAGACAGGAAGGGG[C/T]TGAAACAGCAGTCTC	25897
rs760704081	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100327647	GTGGTCATAACCTGG[A/G]AAATCCTGAGTGGAT	25897
rs760769373	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100298013	TTAAATTACTAAGAC[G/T]CAGTTTCTTCAATTA	25897
rs760771192	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100312479	GCAGTCCCAGCTACT[C/G]CAGGGGGCTGAGGCA	25897
rs760793228	snp	A/G	1.64787e-05	0.00287038	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264715	ACGATTACAGACAAC[A/G]TTACACCACCTGCTA	25897
rs760811251	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100329977	TTCAAGTAGAGCTTA[A/G]ATGGTCATGTAAGGG	25897
rs760834409	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100283332	CAGATATTTTTATTC[A/G]AGGCAGCTTCTATGC	25897
rs760889545	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310271	CTTGCGCACGTTCGT[C/T]CCGCGCCCGCGCAGG	25897
rs760904897	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100318662	GTGAAATGATTCCAA[A/G]CAAAAGCAAACAAAC	25897
rs760904952	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100331322	TGCAACTCCTTTCAA[A/G]ACATCTTATTTAGAA	25897
rs760961023	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259096	GGACCACTTGGTGGC[A/G]CTAGATTTACCTTCA	25897
rs760964388	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100290702	GGATACATTCTGAGA[A/C]ATGTGTCATTAGGTG	25897
rs760985973	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100324180	CCCAATCTAGATTTA[C/T]AAAGTTAGTTCCATA	25897
rs760997435	snp	A/G	1.65781e-05	0.00287902	intron-variant	RNF19A	GRCh38.p7	8:100264820	GGGTGGGGGATTAAA[A/G]AGAAAATACATTACA	25897
rs761052277	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291549	CCAATAAACATCTAA[C/T]CATAAACACTTCAGC	25897
rs761052726	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100323039	GAGCACAGGCTGCCG[A/G]AAAATGTTGCCAATA	25897
rs761059534	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100260583	CCAACATTTGCCTTT[C/T]TAAAAAGAGGTAGTA	25897
rs761137066	snp	A/C	1.73975e-05	0.00294931	intron-variant	RNF19A	GRCh38.p7	8:100275211	CATAAAACAAGAGAT[A/C]CTCATTTCAAAAAGT	25897
rs761193884	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272890	TTGTTTTTGGAAACA[A/G]GGTCTCACTCTGTCA	25897
rs761213291	in-del	-/TTG			intron-variant	RNF19A	GRCh38.p7	8:100315650	TTCTTCTTCGTCGTC[-/TTG]TTGTTGTTGTTGTTG	25897
rs761251058	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100299889	TCTCCAATTTTGGAA[G/T]CTCATTTGTCTCTTT	25897
rs761251835	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310916	TCTACACTAGTCTTG[A/G]TATTCTTAGTTGAAT	25897
rs761304424	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100261388	CAGGCGTGAGCCACT[G/T]CACCTGGCCCCAAAT	25897
rs761325399	in-del	-/AAAAC			intron-variant	RNF19A	GRCh38.p7	8:100329429	TGATACAGTGCTGCA[-/AAAAC]AAAACAAAACAAAAC	25897
rs761340979	snp	C/T	1.65173e-05	0.00287374	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258773	GGGGAATTTTCCAGA[C/T]GGTCATTTTCTACCT	25897
rs761362681	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100318327	TAAGATTTAAAAGGA[C/T]GTATTTTATATACTT	25897
rs761367222	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100335079	GACAGAGCTAGAACA[C/T]TGTGTCAAGGAAAAG	25897
rs761378334	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100266444	AATAGTTTTGTTTTC[A/G]GCAAAGCCTTGCTTT	25897
rs761419050	snp	A/G	8.25825e-05	0.0064253	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274988	CTATAACTAATGGAT[A/G]AAGAACGTATAGTTC	25897
rs761477443	snp	A/G	0.000214456	0.0103529	intron-variant	RNF19A	GRCh38.p7	8:100260003	TACTTCCAACCTTAA[A/G]GGGGGGTATGAAATC	25897
rs761534541	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100296478	CCTAGTAAAGTAAAA[A/C]TATAACAAGCACATT	25897
rs761560482	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100296905	CATGGCTAAACAAAG[A/T]CTCCGATTCATCACA	25897
rs761622408	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283720	GTCAGATACAGAAAA[C/T]GTTCATACCTATAAA	25897
rs761687108	in-del	-/AACAAC			intron-variant	RNF19A	GRCh38.p7	8:100312933	TCTCAAACAAAACAA[-/AACAAC]AACAACAACAAAAAT	25897
rs761688747	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100263916	GTACTTCTGAATGAA[C/T]ACTATTAGGCCTAGT	25897
rs761704501	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100284540	ATCACGGACAATTAT[C/T]TGTTAAATTTATATA	25897
rs761713357	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100269401	CACTGTAAATTATAT[A/T]AACAAGATACTGATA	25897
rs761733687	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100328626	ACAGGCACGCGCCAC[C/G]ACACCCAGCTAATTT	25897
rs761780648	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100267336	AATAAGTAAAAGTAC[A/C]TACAACACCTATGAC	25897
rs761833362	snp	C/T	1.64827e-05	0.00287073	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288071	GAACCCATTTGCCGA[C/T]GTAAACTCATGTCTA	25897
rs761846418	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100285838	ATTTAGAGGAATGTA[G/T]GAAGCACCTCTTGCA	25897
rs761854844	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316346	CCACAGTGTGGAAGG[A/G]GACCCCAGTGGGTTG	25897
rs761859277	in-del	-/GTTTT			intron-variant	RNF19A	GRCh38.p7	8:100279365	ATATTTGATTGCCAG[-/GTTTT]GTTTTGTTTTGTTTT	25897
rs761918462	snp	A/T	1.70848e-05	0.00292269	intron-variant	RNF19A	GRCh38.p7	8:100268745	ATACACCTAAAGATT[A/T]AGAATAAGATAATGG	25897
rs762010287	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100287341	AAGATAGGATCACTG[C/T]CTTTAACACCTAGCA	25897
rs762035522	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100306349	ATTGAGAGTTTCATG[C/T]AACAAAACCTTTCCT	25897
rs762055889	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100326359	AGTTCCTAACACAGC[A/G]ATTCCCAGCATTTTC	25897
rs762112376	snp	A/G	6.59315e-05	0.0057412	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268857	TATTAAAGCGATTCC[A/G]ACAGGAGCACCAACC	25897
rs762114396	snp	C/G/T	4.94176e-05	0.00497059	synonymous-codon, missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259018	TCTCGTCTCATTTAT[C/G/T]TTCATGTTACCCTTT	25897
rs762122401	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100312536	GGTCAAGGCAGCAGT[A/G]AGCCCTGGTCACACC	25897
rs762143144	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257742	GCCATTAAAACCCAG[G/T]CGATCCCAAAGGCAC	25897
rs762167828	snp	C/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259100	CACTTGGTGGCACTA[C/G]ATTTACCTTCAGGCA	25897
rs762182772	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100279104	GAAAATGGCTGCTTA[C/T]AGAGAACAAGATTTT	25897
rs762185957	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100274825	AAGAATGAGTGCTTC[C/T]GGGATAGAAATGCAC	25897
rs762214358	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100299380	CTCCCAAGTATTAGT[A/G]TACTCTTCTTAGTAA	25897
rs762220677	snp	A/G	1.6477e-05	0.00287024	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287647	TTCAGTACATTCTGG[A/G]CAACTAATATTAACT	25897
rs762222864	snp	G/T	1.66427e-05	0.00288462	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259219	CTTTGACTCAATATC[G/T]ACTTGCACCTCCATA	25897
rs762275745	snp	A/G	3.29522e-05	0.00405894	missense, intron-variant	RNF19A	GRCh38.p7	8:100261729	CTATGCTTGGGTTGT[A/G]TCTTGCTTCTGCTAC	25897
rs762347262	snp	A/G			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336345	TGAAATAGGTCAGGA[A/G]CTGCCAGTTTGCAAA	25897
rs762354816	snp	A/G	1.64754e-05	0.00287009	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287836	TCCATTGTCAGAAGA[A/G]GTATTTGTAGAGAAA	25897
rs762364777	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100313768	CCAATAAAGATGTCA[C/T]AGTTCTTTGAACCAA	25897
rs762480754	snp	G/T	1.64846e-05	0.0028709	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275031	TCTGGGCTCTCTCTT[G/T]TCGAGCAGCATCACA	25897
rs762482410	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100291814	CTGATGGTCAAAATA[C/G]TAAATGTAAGAGCAG	25897
rs762488788	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100306054	CTGGCTCCCTCCTTA[G/T]GGCTCACTTCTACCA	25897
rs762549381	snp	C/T	1.64982e-05	0.00287208	missense, intron-variant	RNF19A	GRCh38.p7	8:100261561	TAAAACAGTTTACCA[C/T]GGCACTTCCTGACAG	25897
rs762572010	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100293064	CCTCGAGTGCAGTTC[A/G]CAATACTCCTATGAG	25897
rs762604775	in-del	-/ACAA			intron-variant	RNF19A	GRCh38.p7	8:100296993	GAAAACAAAAATCAT[-/ACAA]ACAAAGGTTAATCAA	25897
rs762605185	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326383	CATTTTCCATTCTTC[C/T]AAGTCCCTAATGCCC	25897
rs762617155	in-del	-/AA			intron-variant	RNF19A	GRCh38.p7	8:100318678	CAAAAGCAAACAAAC[-/AA]GAGATTAAATTAATT	25897
rs762686296	snp	A/C	6.75185e-05	0.00580988	intron-variant	RNF19A	GRCh38.p7	8:100275187	CAAGAAAAATGATTT[A/C]AAATGTGACATAAAA	25897
rs762719762	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100315626	TTCCCAGCAGGGTCA[C/T]GGAAATTTTTCTTCT	25897
rs762724217	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100262995	TGAAGGGAAGAAGAG[A/G]TTTTAGAGCCAAGAA	25897
rs762753638	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258206	GCCTCAAGTTTTCTT[C/G]ATTTGAATGCTGTAG	25897
rs762762948	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100329626	AGCATGAATCCAAAG[A/G]CAGACAACTAGGTTA	25897
rs762766801	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100269597	GAAAATTAAATGAAA[A/G]TATTTATGGGTCTAG	25897
rs762772823	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100313125	CTAATTCATTTAACA[C/T]CAATTCGATAAACAT	25897
rs762800292	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288664	GAAAGGGCTCTAACA[C/G]CGCCAGATATAATGA	25897
rs762837103	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285736	CTCATGGGTTCAAGT[C/T]ACCTTCCCGTCTTGG	25897
rs762852363	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100271261	TAAGCAGCCAGACCA[A/G]GACAATTGATAATTA	25897
rs762905371	snp	A/T	1.70452e-05	0.0029193	intron-variant	RNF19A	GRCh38.p7	8:100268988	TAACTGCTGCAAAAC[A/T]CCACAATAACAAATT	25897
rs762916906	in-del	-/C	1.64743e-05	0.00287	frameshift-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259028	TTTATCTTCATGTTA[-/C]CCTTTTTCCTCAGTT	25897
rs762941358	snp	C/T	1.97971e-05	0.00314613	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288180	GTTCTTGCATTCACA[C/T]TAAGTCATGATGTAA	25897
rs762974707	snp	A/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305337	AGGTGTATGCAATTC[A/T]GTATTTGGCCTCAAA	25897
rs762992709	snp	A/G	1.64822e-05	0.00287068	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268874	CAGGAGCACCAACCA[A/G]TGTTCCCAGTTGCCA	25897
rs763009786	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326793	ACACTTTAAACAGTC[C/T]GTATCAAACACAAAA	25897
rs763012920	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100328479	TTTTTGTTTGTTTGC[-/T]TTTTTTTTTTGAGAC	25897
rs763037362	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100321203	CTTGGCAGCATTTTA[C/T]CCACAGTAGAAGTTC	25897
rs763069117	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100308851	CGCCGTCTTTTCTAA[A/C]GTCACCCCAACAGAA	25897
rs763131031	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307507	ACCAAAAAATTTCTA[C/T]ATAAATCTAAATAAG	25897
rs763134323	snp	C/T	1.68596e-05	0.00290336	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259233	CTACTTGCACCTCCA[C/T]ACTGTTGCCTTCTCT	25897
rs763182817	snp	C/T	9.88631e-05	0.00703006	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287692	TTCTATCCTTAAATA[C/T]TGTCGTAAGCAATCC	25897
rs763185763	in-del	-/AATAGCTCCTTCTATAAG	1.88991e-05	0.00307396	intron-variant	RNF19A	GRCh38.p7	8:100269846	TTACATTTACATATA[-/AATAGCTCCTTCTATAAG]CTTACCTTAGATAAT	25897
rs763228121	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100264852	TTTAACTTAGTTGAA[A/G]AAGATCTATACTTGC	25897
rs763234689	snp	C/T	1.64749e-05	0.00287005	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287864	AAAATGGAGTTCTTA[C/T]CAGTACACATTTCAG	25897
rs763261147	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100314183	CACGTGCCCAGCCGA[C/G]AACTACTCTTTATTG	25897
rs763296068	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100279873	TTTTGCCATGTTAGT[C/G]AGGCTGGTCTCGAAC	25897
rs763371111	in-del	-/ATTT			intron-variant	RNF19A	GRCh38.p7	8:100292797	TCTTATTTTTGAGAC[-/ATTT]ATTTATTTATTTATA	25897
rs763440155	snp	C/T	1.64996e-05	0.0028722	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264090	TCATCAAATTCAATC[C/T]TAACTCCTTTTCCAT	25897
rs763495362	snp	C/T	1.65217e-05	0.00287412	intron-variant	RNF19A	GRCh38.p7	8:100264657	GTAATTAGTACTTTT[C/T]AGCATTTTCTTACCT	25897
rs763508641	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100302294	AGAAAGATGACGATG[A/G]CACATCAGTGAAGGT	25897
rs763604442	snp	A/G	3.84209e-05	0.0043828	intron-variant	RNF19A	GRCh38.p7	8:100269843	AAATTACATTTACAT[A/G]TAAATAGCTCCTTCT	25897
rs763612642	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100267256	AAGATATATTACATA[A/C]ACTTTCCTAAATCTC	25897
rs763616690	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100334228	AACATAATGCTTCAC[A/G]GTTCTGCCACCATTT	25897
rs763687952	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100290715	GAAATGTGTCATTAG[C/G]TGATTTTGTCGTGTG	25897
rs763699889	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100318944	TGGCCAGAAGCACAT[G/T]GCCCAGAGCAATCCC	25897
rs763740140	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100259264	GAAATATAAGAGTAA[C/G]AAATACAAACATAAT	25897
rs763770619	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100275841	TTTTAACTGTCAGGT[A/C]ATGGCATACTGTGCC	25897
rs763772233	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100262719	CTATGGACTAGTGAA[C/T]AGAAGCTGAGAAGTT	25897
rs763820433	snp	C/G	1.68886e-05	0.00290586	intron-variant	RNF19A	GRCh38.p7	8:100270021	ATCATCAGCTATTGG[C/G]AACACAGAGAAATCT	25897
rs763848263	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100294853	TTTTTAAAACGATCC[C/T]TTAAAAGATTTTCTT	25897
rs763853976	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100281324	TGCCAAGTAAAATTA[A/G]AGTGGTTTTTGTTTT	25897
rs763878086	in-del	-/GC			intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309352	AGCACGGCTTGCGGG[-/GC]GATGTCCCGGCTCCA	25897
rs763929734	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100278253	CTCATAGTTCTGCAC[-/T]TGTGCTTGACTAATG	25897
rs763933213	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100308455	TAAATAGAGAAGTAT[G/T]TACATTTTAACTCAA	25897
rs763944525	snp	C/T	3.30055e-05	0.00406222	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259891	TCAGAATGGATCCTG[C/T]CATTGCTTTGGTGCT	25897
rs764056485	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100285221	ACAATGTGGCAGTAG[A/G]TTAATCATTCACCTA	25897
rs764058122	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100327731	CTTTAGGAAAACATC[C/T]GGTTCCTCTTTTGAA	25897
rs764092903	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100280676	GTAGTTTTTTCTCAC[A/G]CTAACACTTATTGAG	25897
rs764112433	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100296615	TTCTAGGCACAGGAT[A/G]GATCCACAGCTTTCA	25897
rs764139989	snp	A/G	6.58989e-05	0.00573978	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287971	CCTCCGAAACAGGGA[A/G]CCTATTGAAATTCTT	25897
rs764159783	in-del	-/AAAAC			intron-variant	RNF19A	GRCh38.p7	8:100329433	CAGTGCTGCAAAAAC[-/AAAAC]AAAACAAAACAAAAC	25897
rs764237470	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100331362	AGATATAGGCCAGGT[A/T]TGGTGGCTCATGCCT	25897
rs764252406	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100299054	AATTTGAATGCTGCA[A/T]ATCCAAAGGAAAACA	25897
rs764253148	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259003	TGCATCCATGTCCTC[C/T]CTCGTCTCATTTATC	25897
rs764296636	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100324107	AGATGACTTTGTTCA[A/G]AGAAAATTCCCACAC	25897
rs764299825	snp	C/T	4.94344e-05	0.00497139	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264726	CAACGTTACACCACC[C/T]GCTATGGCCAAATTC	25897
rs764323097	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100319690	ACACACCACCATGCC[C/T]GGCTAATTTTTGTAT	25897
rs764326616	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100300130	GCACAATAAGCAAAA[C/T]GTGTCTGTTTCCCTT	25897
rs764329758	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285898	AAATCACACTCTTTC[C/T]GTAGATGAAACATAA	25897
rs764352892	snp	C/G	3.29777e-05	0.00406051	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258817	AACAGTAGCAAAGCG[C/G]GTGTGATAATCACTG	25897
rs764385384	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100271462	AGCAGCATGTTAATC[A/G]ATAAACTTTCTCATT	25897
rs764389173	snp	A/G	1.71372e-05	0.00292717	intron-variant	RNF19A	GRCh38.p7	8:100268734	ATACTAAAAGAATAC[A/G]CCTAAAGATTTAGAA	25897
rs764401708	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100305423	ACATGTCATACAAAA[C/T]GCCCCTAGAGCTACG	25897
rs764408643	snp	C/G	1.64803e-05	0.00287052	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275058	CACAGGTCTGGTTGG[C/G]GTGCCAAATCTGTTT	25897
rs764423398	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100276949	TGATATTGTTCTATA[A/G]CTTGTGCAAAATGGC	25897
rs764477460	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100269522	GCATATTTTTAGGCA[C/T]CAATTATCTGATTAT	25897
rs764511373	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100260603	AAGAGGTAGTATATA[C/G]CACTATAACTTAAGA	25897
rs764522313	in-del	-/CCTTAG	3.38627e-05	0.00411463	splice-donor-variant	RNF19A	GRCh38.p7	8:100269868	CCTTCTATAAGCTTA[-/CCTTAG]ATAATGCAAATCTGA	25897
rs764550613	snp	C/T			intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100309317	CTCCGAACACAGCTC[C/T]CCTCCCTAAGGCCCC	25897
rs764559027	in-del	-/TTG			intron-variant	RNF19A	GRCh38.p7	8:100330652	AATATCCTGATGATA[-/TTG]TTGAGTCTCTGGACT	25897
rs764601290	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100261416	AATTTCATTTTTAAC[A/T]TTACTATTTTGAACC	25897
rs764604471	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310985	TTTATTCTCTTCAAG[A/G]TTTAGATCACTCTAA	25897
rs764614688	snp	C/T	1.75523e-05	0.00296241	intron-variant	RNF19A	GRCh38.p7	8:100287495	AATCAAACATTATCT[C/T]CTTACCCACAGTCTG	25897
rs764692097	snp	A/G	1.69746e-05	0.00291325	intron-variant	RNF19A	GRCh38.p7	8:100270032	TTGGGAACACAGAGA[A/G]ATCTATTAAGTACAT	25897
rs764700005	snp	A/G	4.94784e-05	0.00497361	missense, intron-variant	RNF19A	GRCh38.p7	8:100261584	CCTGACAGACTCCCC[A/G]TTATACTGGCTCCAG	25897
rs764737643	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100335225	CAGCAATAATACTAA[C/T]AGTTAACAATTTTTA	25897
rs764751253	snp	C/T	1.64914e-05	0.00287149	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259911	GCTTTGGTGCTGGCA[C/T]TATCACTAACTGTTC	25897
rs764777063	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100290915	ATTTCTTTGGCTCTC[C/T]GATATCCTGCCAGTG	25897
rs764778067	snp	C/T	4.94727e-05	0.00497332	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268906	AATATTTTCTTCTTT[C/T]GGCTCCAGGGTTTCT	25897
rs764804572	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100279121	GAGAACAAGATTTTT[A/G]AGATTTATCCAAACT	25897
rs764805929	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305236	TGGGAAAGACAGTAA[C/G]GCGCAAAGTCATTTT	25897
rs764860428	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100277405	CAATCTCCACCTCCT[A/G]GGTTCAAGCTATTCT	25897
rs764890540	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100284119	GGAAATACAGATGAA[G/T]AATAATAAGTAAGAG	25897
rs764891138	snp	A/G	1.6513e-05	0.00287336	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274990	ATAACTAATGGATGA[A/G]GAACGTATAGTTCTC	25897
rs764907706	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100332703	TGCAAATTTGTTAAA[A/T]TGTTATCTCATTTTC	25897
rs764944412	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100267255	GAAGATATATTACAT[-/A]AACTTTCCTAAATCT	25897
rs764969844	in-del	-/AA			intron-variant	RNF19A	GRCh38.p7	8:100297246	CTAGATGTACAATCT[-/AA]ATACCTTTCAATTAC	25897
rs765043965	snp	A/T	1.64836e-05	0.0028708	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288080	TGCCGATGTAAACTC[A/T]TGTCTAAAATGCTTG	25897
rs765128562	snp	C/T	1.64765e-05	0.00287019	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287990	ATTGAAATTCTTCTT[C/T]TTTTGGGTGCCTTTT	25897
rs765145703	in-del	-/CT			intron-variant	RNF19A	GRCh38.p7	8:100259524	TCAGATACAATTCCC[-/CT]GTTTAAAGTGTACAA	25897
rs765187918	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100285977	TATAATGACTCACAA[A/G]AAGTTTTTTTAAAAC	25897
rs765280441	snp	A/G	3.39893e-05	0.00412232	intron-variant	RNF19A	GRCh38.p7	8:100268757	ATTTAGAATAAGATA[A/G]TGGACTAACAAGAAG	25897
rs765365666	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100324779	TGATTAAAGGCATTG[A/C]TCTATCTTTTTTCTT	25897
rs765376677	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100306363	GTAACAAAACCTTTC[C/T]TAATAGGACTTCTAA	25897
rs765432777	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100321146	TGCCACATCAATTGA[C/G]TCTTCCTTCCACAAA	25897
rs765466195	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307440	CCTGTAGATTAAAAA[C/T]GACAACAACAACAAA	25897
rs765477120	snp	A/G	6.59294e-05	0.00574111	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268863	AGCGATTCCGACAGG[A/G]GCACCAACCAGTGTT	25897
rs765510663	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257069	CAGAAGGCAGCAGTA[C/T]ATTAGTATTTACATT	25897
rs765517264	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100298330	CACGAATTTCTCAAA[C/G]GTAAATTATATAAAT	25897
rs765536516	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259104	TGGTGGCACTAGATT[C/T]ACCTTCAGGCAAGCC	25897
rs765539158	snp	C/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337699	AGCGAAATTTCTGAA[C/T]TTCCGAGCTGTGATA	25897
rs765571716	snp	C/T	1.66112e-05	0.00288189	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287541	TACAATCAGGATCTG[C/T]AACAAGCCACCGTCT	25897
rs765595161	snp	C/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337686	GCATTTTGACCTGAG[C/T]GAAATTTCTGAATTT	25897
rs765600107	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100273363	CATCTTACTTTGCAT[C/G]TATACCAAACCAATA	25897
rs765603515	in-del	-/A	1.67284e-05	0.00289205	intron-variant	RNF19A	GRCh38.p7	8:100268954	CTGATGGACTAACGG[-/A]AAAAAATTATAATGT	25897
rs765630670	snp	C/T	1.64773e-05	0.00287026	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287658	CTGGGCAACTAATAT[C/T]AACTCTGCTTTCAGA	25897
rs765669170	snp	C/T	1.65037e-05	0.00287256	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264076	TTATATCATTTTCAT[C/T]ATCAAATTCAATCCT	25897
rs765690450	in-del	-/TTCCTTTAATTTAAAAAATACTTTCAATTTTTTAACAGTTTT	2.66365e-05	0.00364932	intron-variant	RNF19A	GRCh38.p7	8:100259804	TAATGATAGGAATTA[lengthTooLong]TTCCTTACTTGTCCA	25897
rs765701622	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100331547	GAGGCTGAGGCAGGA[A/G]GATTGCTTGAGCCCA	25897
rs765727710	snp	C/T	1.64757e-05	0.00287012	missense, intron-variant	RNF19A	GRCh38.p7	8:100261735	TTGGGTTGTGTCTTG[C/T]TTCTGCTACTGATGT	25897
rs765738038	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100330170	GAGTTTGCTCCCACA[A/C]TCTCCCCAACCTTCT	25897
rs765779046	snp	C/T	1.79252e-05	0.0029937	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258535	TTGTACAGTGGTAAT[C/T]ATTCTGCAGCATTTA	25897
rs765837586	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100316588	TAGATACAGAGCGTC[C/G]ATTGGTGCACTCACA	25897
rs765897368	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100325479	CACCTTGTCACCTCT[A/G]GGTCCTCCCTTTTCA	25897
rs765960757	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100263028	TGGCTGTAGACAAGT[G/T]AAGCTTGAAATTCTT	25897
rs765962083	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100293089	TATGAGAAATCATTG[A/T]TGCCACTGATCTGAC	25897
rs766046359	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100299507	GCTCACGCCTGTAAT[C/G]CCGGCGCTTTGGGAG	25897
rs766050731	snp	G/T	1.65075e-05	0.00287289	intron-variant	RNF19A	GRCh38.p7	8:100260012	CCTTAAAGGGGGGTA[G/T]GAAATCACCAAAATT	25897
rs766056908	snp	A/G	1.64741e-05	0.00286998	intron-variant	RNF19A	GRCh38.p7	8:100275199	TTTAAAATGTGACAT[A/G]AAACAAGAGATACTC	25897
rs766086035	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100318630	CAGCATTCCTCAACT[A/G]CATTATTATCTAGCG	25897
rs766104272	snp	A/G	1.64961e-05	0.00287189	synonymous-codon, intron-variant	RNF19A	GRCh38.p7	8:100261565	ACAGTTTACCATGGC[A/G]CTTCCTGACAGACTC	25897
rs766109764	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100269638	CAGGGTATTACATAC[C/T]TACTAGCATTCTAGT	25897
rs766146507	snp	C/T	3.29728e-05	0.00406021	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288090	AACTCATGTCTAAAA[C/T]GCTTGTTAGAATTGA	25897
rs766174070	snp	C/T	3.29614e-05	0.00405951	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268884	AACCAGTGTTCCCAG[C/T]TGCCACAATATTTTC	25897
rs766195743	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304216	ATTTGCCCACCTTGG[C/T]CTCCCAAAGTGCTGG	25897
rs766198299	snp	C/T	4.10568e-05	0.00453064	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288188	ATTCACATTAAGTCA[C/T]GATGTAAGAATATCC	25897
rs766240360	snp	A/G	1.65877e-05	0.00287986	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268788	TATGCATTTTACCTT[A/G]CGGCCCACATACACA	25897
rs766319294	snp	A/C/T			intron-variant	RNF19A	GRCh38.p7	8:100275576	CTTTTAAGTAGGATA[A/C/T]CAAATTGCATTTAGC	25897
rs766322330	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326893	CAAGGTTTATTTAAG[C/T]GTTATCTTATACTTC	25897
rs766342388	in-del	-/TTTTC			intron-variant	RNF19A	GRCh38.p7	8:100282645	AGTCCCATGTACTTG[-/TTTTC]TTTTCTCTGGATAAA	25897
rs766348649	snp	C/T	1.70723e-05	0.00292162	intron-variant	RNF19A	GRCh38.p7	8:100268990	ACTGCTGCAAAACAC[C/T]ACAATAACAAATTAG	25897
rs766377597	snp	A/G			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336401	GTTAGGGGCAAGCCC[A/G]GAAACCGAACGACAC	25897
rs766517146	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257505	ACTTGGTACAAGTTC[G/T]GCACCGTGCTTTGAT	25897
rs766534732	snp	C/T	1.70609e-05	0.00292065	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259242	CCTCCATACTGTTGC[C/T]TTCTCTGAAATATAA	25897
rs766545793	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287695	TATCCTTAAATATTG[C/T]CGTAAGCAATCCACA	25897
rs766561269	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100308936	TATTTATATCTCCAA[A/G]GGTCAATGGGAAAAA	25897
rs766604789	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100259266	AATATAAGAGTAACA[A/G]ATACAAACATAATTG	25897
rs766605182	snp	A/T	1.64846e-05	0.0028709	intron-variant	RNF19A	GRCh38.p7	8:100261770	TCTAAATGCAAATAT[A/T]CCAAAGAAACTAAGT	25897
rs766695018	snp	A/G			intron-variant, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100300608	CAGTGAGCTATGATC[A/G]CACCACTGTATTCCA	25897
rs766753508	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100287418	TCTCCAGCATGTAAA[A/C]ATTTTTCTTTTGAGT	25897
rs766796048	snp	A/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289385	AAAATCAACAGACAG[A/T]ATTAAGGGTATGGGA	25897
rs766821126	snp	A/G	4.94482e-05	0.00497209	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288069	CTGAACCCATTTGCC[A/G]ATGTAAACTCATGTC	25897
rs766839946	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100321356	TCCATCTAAAGAAAC[C/T]ACTTTCTTTCCTCTT	25897
rs766890277	snp	A/C	1.64849e-05	0.00287092	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258639	TTAGTGCATCGCCAA[A/C]ATATAAATCAACATT	25897
rs766951388	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100333137	GGTGGGTTAACATGG[G/T]AGTGGGTTTGTCACA	25897
rs766983470	in-del	-/A	3.50018e-05	0.00418326	intron-variant	RNF19A	GRCh38.p7	8:100270065	AACTGGTCTAAAAAT[-/A]ACTTCTAGCAGTTTA	25897
rs767007177	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100316199	TCCTTCCTCCCAGTG[C/G]GCTTGTGGTCTCGCT	25897
rs767021285	in-del	-/CTG			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257352	ATCATTGAGGTTAAC[-/CTG]CTGCTTTTATTTAAG	25897
rs767021685	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100315435	AATGGGAGCTTGGGG[A/G]CTTTAGTCTCCACCA	25897
rs767053746	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100314318	TATTCTGATTGCTTT[A/G]TAAGTATTAAGCCAC	25897
rs767084223	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100263242	CAAAGATTAATGAGA[C/T]GGACTGGCCAGGAAA	25897
rs767095998	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100300915	ACAAAAAAACTAGTC[A/G]TGTAAAGGTCCCTGT	25897
rs767120559	snp	A/C	2.25772e-05	0.00335977	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288206	TGTAAGAATATCCTA[A/C]TTGGTTCCTTCAGAG	25897
rs767128550	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288929	GCCGGGTGTGGTGGC[A/G]GGCCCCTGTAGTCCC	25897
rs767173476	snp	C/T	1.64846e-05	0.0028709	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268896	CAGTTGCCACAATAT[C/T]TTCTTCTTTCGGCTC	25897
rs767187608	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100302471	AGAAGTTCATTTTTA[C/G]ACATTTATACTTGAG	25897
rs767192609	snp	C/G	1.64743e-05	0.00287	missense, intron-variant	RNF19A	GRCh38.p7	8:100261714	CAACACTTCCCTCCC[C/G]TATGCTTGGGTTGTG	25897
rs767206716	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100264962	ATTCTCACAAATAAT[C/T]TGCTCCTTATTAATT	25897
rs767230833	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100262210	GTATTAAGGAGTCAC[C/T]TATTTGCACCAATAT	25897
rs767311401	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100292293	GCTTTGATAGCAAAG[A/G]TATTTTTAGTATTGT	25897
rs767334361	snp	A/G	1.74309e-05	0.00295214	intron-variant	RNF19A	GRCh38.p7	8:100259256	CCTTCTCTGAAATAT[A/G]AGAGTAACAAATACA	25897
rs767369567	snp	C/T	4.0966e-05	0.00452563	intron-variant	RNF19A	GRCh38.p7	8:100269824	TATTTTGTCTTACAA[C/T]ATAAAATTACATTTA	25897
rs767451204	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100260554	GGATTATAGGTATGA[A/G]CCACTGAGCCCAACC	25897
rs767459028	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100280508	CAGTATTTTTTAAAT[A/G]GAAAAGGTAAGATGT	25897
rs767461382	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100296894	AAAACAACTTTCATG[A/G]CTAAACAAAGTCTCC	25897
rs767493497	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100294731	GGATATCTTCATCTA[A/G]GCTTTGAGATACAGT	25897
rs767519899	snp	A/G/T	3.31012e-05	0.00406813	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259865	TTACTTGTCCAATGG[A/G/T]ATGTAGGAATTCAGA	25897
rs767558542	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100332190	CTGATTTGGTTTGGC[G/T]CTGTGTCCCCATGTA	25897
rs767564688	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280346	AAGATTATACATATG[C/T]AGTGTTTGTGTGTCT	25897
rs767644749	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100277456	AGCTGGGACTACAGG[C/T]GCCCACTACCACGCC	25897
rs767679659	snp	A/T	1.64746e-05	0.00287002	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287871	AGTTCTTATCAGTAC[A/T]CATTTCAGAATGTAT	25897
rs767691922	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100297903	GGTAGTGATAGAGTA[C/T]ATTTTGTTGAGTGAG	25897
rs767726348	snp	C/T	1.65971e-05	0.00288067	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264157	GAGAAATTGGAACTA[C/T]GCCATAGACATAAGC	25897
rs767759248	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100283191	TCACATGGGATGACA[A/G]GGATAATGTGCGCTG	25897
rs767854511	snp	C/T	0.000296721	0.0121767	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275132	GTTAATTTTGGACAG[C/T]TGGCACATCCAAATG	25897
rs767903773	in-del	-/AAA			intron-variant	RNF19A	GRCh38.p7	8:100268685	GATACCCTTTGTCTA[-/AAA]AAAAAAAAAAAAAAA	25897
rs767903859	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100269264	AGTCAGTTTAATAGT[A/G]AATTAATGCAAAACA	25897
rs767911056	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100334065	TTCTTGATTTTGCTC[A/T]TTCTGTTCACTGTGC	25897
rs767919807	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100276569	CCAGCCTGGTCAACA[C/T]GGCAAAACCCCATCT	25897
rs767924013	snp	A/C/T	3.3004e-05	0.00406216	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258805	AGGAAGAATGTTAAC[A/C/T]GTAGCAAAGCGGGTG	25897
rs767979637	snp	A/G	4.94222e-05	0.00497078	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258980	GTGCTTTGTTGTTCT[A/G]ACAACTGTGCATCCA	25897
rs767983948	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100321579	TGTTGATATTTTGAA[C/T]GCTTCCCATGAATGA	25897
rs767988636	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100275619	TTATAAAAAACCATA[G/T]TAAATTAGTACAGTA	25897
rs768080460	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100259500	CCTTTTTTTAAAGAA[A/C]AGCTTTATTCAGATA	25897
rs768102604	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100267087	ATTTTGTAACAATTA[A/G]TAGCCATTTTACAAC	25897
rs768155750	snp	C/G	1.64814e-05	0.00287061	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275047	TCGAGCAGCATCACA[C/G]GTCTGGTTGGGGTGC	25897
rs768162692	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100294567	GATTTATCCTATTTC[C/T]GGCCACTTAACTTCC	25897
rs768163849	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100309041	GGTTAATGAACCCTA[A/C]ACTTCTTTTTCTTCT	25897
rs768218121	snp	A/G	6.58935e-05	0.00573955	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258934	AGGCATACTGTCACT[A/G]AGGGATGGAGCCTCA	25897
rs768226274	in-del	-/TTT			intron-variant	RNF19A	GRCh38.p7	8:100291968	AAAGAGGACTAAGTC[-/TTT]TTTTTTTTTTTTTTT	25897
rs768231220	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100320435	GTTTCTCTAGGTTAT[-/A]TGCCTAGAAGCAGAA	25897
rs768274021	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100329262	ATATACACACATACA[C/T]GTACACAAACACACA	25897
rs768295902	snp	A/G			missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258816	TAACAGTAGCAAAGC[A/G]GGTGTGATAATCACT	25897
rs768327869	snp	C/T	1.65168e-05	0.00287369	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258765	ACTGATGTGGGGAAT[C/T]TTCCAGACGGTCATT	25897
rs768342419	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100270854	GGTTACAATGCACAA[A/T]GGCGTCAAGTTAAAA	25897
rs768400186	snp	G/T	1.65332e-05	0.00287512	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274980	ACTCTTGACTATAAC[G/T]AATGGATGAAGAACG	25897
rs768462769	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100323601	TAAAATTTCATCTAC[A/C]TTTGCCAGGGGAATC	25897
rs768524873	in-del	-/CC	1.64754e-05	0.00287009	frameshift-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259106	GTGGCACTAGATTTA[-/CC]TTCAGGCAAGCCACT	25897
rs768530277	in-del	-/ATCCTTT	1.64732e-05	0.0028699	frameshift-variant, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264109	TCCTTTTCCATTGCC[-/ATCCTTT]TGCTGAGACTCCACA	25897
rs768560436	snp	A/G	0.000296809	0.0121785	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259996	CTGCTTGTACTTCCA[A/G]CCTTAAAGGGGGGTA	25897
rs768613796	snp	A/C	1.65236e-05	0.00287429	intron-variant	RNF19A	GRCh38.p7	8:100261535	CAAACCAAACCAAAA[A/C]ACACACCTGTTAAAA	25897
rs768668517	snp	C/T	3.2956e-05	0.00405918	missense, intron-variant	RNF19A	GRCh38.p7	8:100261653	CGGATGGCTCCTATT[C/T]GATCCATGTGGCTTC	25897
rs768708931	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100261220	CTACCTCAGCCTCCC[A/G]ACCAGCTGGGACTAC	25897
rs768748816	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100313714	AAGGCAGAGCAAGAG[C/T]GGAAGTAGGGAGACC	25897
rs768891408	in-del	-/TAAGA			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304420	ATACATCATATACCC[-/TAAGA]TAACAGGCTTTTCTA	25897
rs768917394	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100300212	GAGATTAAAAACTCA[C/T]GTACAAAGGAAATAT	25897
rs768948472	snp	A/C	3.50398e-05	0.00418553	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288155	TATTTAGAGATAAAA[A/C]CTATTTCTTGTTCTT	25897
rs768971122	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100328529	TAGGCTGGAGTGCAG[C/T]GGCACAATCTCGGCT	25897
rs768972028	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100292988	AGATGGAGGTGGGGG[A/G]TGGGAGCAAGGATGG	25897
rs768991899	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100335943	TTGGCCGCTTTCTAT[A/G]CTATGAACCAACGGG	25897
rs769003523	snp	C/G	1.64838e-05	0.00287083	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268849	ATGCCAGCTATTAAA[C/G]CGATTCCGACAGGAG	25897
rs769022514	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100325970	GGGTATATATTTGAG[G/T]TGGACACTTATCCTA	25897
rs769043506	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291650	GGCAGGGCAAAAAGT[C/T]TGCATACACAGAAAA	25897
rs769064442	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100312516	TCATCTCCATAGCCT[C/T]AGGAGGTCAAGGCAG	25897
rs769122984	snp	C/G/T	4.94192e-05	0.00497067	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259098	ACCACTTGGTGGCAC[C/G/T]AGATTTACCTTCAGG	25897
rs769143990	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100325610	GGGTCCTCAAGCCCA[A/G]CCTATATTTGCCATA	25897
rs769180871	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100263569	GAATATAGAACATGC[-/A]CTTTTTAAAAAAGGT	25897
rs769199629	snp	A/G	0.000133775	0.00817738	intron-variant	RNF19A	GRCh38.p7	8:100268953	TCCTGATGGACTAAC[A/G]GAAAAAATTATAATG	25897
rs769211915	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257638	TATTAATCACATTCA[C/T]GTTTATCTATTTCCT	25897
rs769253315	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100286768	CTAATAGTATGCTAC[A/G]TATCACATTAATTGT	25897
rs769332178	snp	A/C/G	3.36362e-05	0.00410088	intron-variant	RNF19A	GRCh38.p7	8:100275178	TTGAAAGAACAAGAA[A/C/G]AATGATTTAAAATGT	25897
rs769339009	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100272278	ATTTAAACACATATA[C/T]AAACATTATACTATA	25897
rs769402284	in-del	-/ATG			intron-variant	RNF19A	GRCh38.p7	8:100285490	TATTAACTATATATT[-/ATG]ATGACATTACCAATC	25897
rs769428980	snp	A/G	3.29473e-05	0.00405864	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259067	TTTGATTTTTTCCCT[A/G]CTGTTGCTTCTTTGG	25897
rs769448743	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100297797	AATTATCTATCTTAC[A/T]CACCTTAAAGCTGGA	25897
rs769476261	in-del	-/TAAG	9.89593e-05	0.00703348	intron-variant	RNF19A	GRCh38.p7	8:100261781	ATATTCCAAAGAAAC[-/TAAG]TAAGTATGATTATCA	25897
rs769484352	snp	A/G			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337250	ACCCAACTGAAGAAA[A/G]CATGTGTGATCAGGC	25897
rs769488802	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293034	TATTCTCATATGGAG[C/T]GTGCCATCTAGATCC	25897
rs769565050	in-del	-/AAG	4.94352e-05	0.00497143	cds-indel, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258846	TGGAACCATGACTAC[-/AAG]AAGTTTTCATGCTTT	25897
rs769578409	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100307076	ATTTAGAAATTCAAC[A/T]TTACTTTGGGCTTTT	25897
rs769611634	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100312041	AGTTTGTTCTTTCCT[C/G]AAAGCATGCTTCTTT	25897
rs769639143	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100331098	TCTCCTATCTAACAC[A/G]TTTATTAAGCACATC	25897
rs769651785	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100274175	GAATTCAGGCAGTCT[C/G]ATTCCAGAGTCATTC	25897
rs769692261	snp	A/G	1.67259e-05	0.00289183	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258593	ACTTTTAATTCCATT[A/G]TCTGATGTGAGTGGT	25897
rs769693521	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100298748	ATACTCATTACAAGT[A/T]ATATTCACTACTCAA	25897
rs769705317	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100329492	TCTTAGGTTGCATTA[A/G]CAAAGCATGTATAGT	25897
rs769735339	snp	A/T	1.64746e-05	0.00287002	missense, intron-variant	RNF19A	GRCh38.p7	8:100261690	CACTCAAACTGCCAG[A/T]CAGCCCACCAACACT	25897
rs769773748	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272103	CGGTAAGGGGACAGA[A/G]GCAGGAGTGGAGAGC	25897
rs769780291	snp	A/G	1.83741e-05	0.00303096	stop-gained, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288165	TAAAACCTATTTCTT[A/G]TTCTTGCATTCACAT	25897
rs769803629	in-del	-/TG			intron-variant	RNF19A	GRCh38.p7	8:100302944	GATTCCTGTTGAGAC[-/TG]GAGGGTATTAAAACA	25897
rs769819408	in-del	-/A			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288283	TGAAAAATAAAAAAT[-/A]AAAAAAATCAAGATC	25897
rs769841652	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100290507	GCCTTTTTCTATGTG[-/T]TTTTTTTCCTCCTAT	25897
rs769845420	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100266504	TAATATATTTTGAAA[C/T]TTTTTATTTTTTCTC	25897
rs769898797	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100302264	ACAGTTTAAAGACTA[C/T]TGAAGTAATCTATGA	25897
rs769900672	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100332835	CCATTTTCCTATTAG[A/G]ATGTTGACCATTATT	25897
rs769930920	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258055	CCACATTGCATATGA[A/G]GAAAAAAAATGAAAT	25897
rs769972275	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100318077	GTGGTATAATACTTC[A/G]GGCCTACATTAAGGG	25897
rs770013902	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257757	TCGATCCCAAAGGCA[C/T]CAAGAATCAATGGGG	25897
rs770115809	snp	A/G	0.000978804	0.0221008	intron-variant	RNF19A	GRCh38.p7	8:100268974	AATTATAATGTAAAT[A/G]ACTGCTGCAAAACAC	25897
rs770136597	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100326263	ACTTCAGAAAAATGC[A/T]GATTCAATTCTCTTT	25897
rs770150816	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100290365	CCTTGGCCTCCCAAA[C/G]TGCTGGGATTATAGA	25897
rs770154963	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100275219	AAGAGATACTCATTT[A/C]AAAAAGTATCCAACT	25897
rs770166837	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100261295	TAGAGATGGGGTTTC[C/G]CCATGTTGCCCAGGC	25897
rs770167226	snp	C/T	1.65138e-05	0.00287343	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269972	CATCATTCATCTTTA[C/T]TATATAAGCAGCACA	25897
rs770175391	snp	C/T	1.66932e-05	0.002889	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259223	GACTCAATATCTACT[C/T]GCACCTCCATACTGT	25897
rs770188384	snp	A/T			missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264713	ACACGATTACAGACA[A/T]CGTTACACCACCTGC	25897
rs770230364	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293992	GACTACCCACATGTT[C/T]GGTCATTATGATATT	25897
rs770236736	snp	A/G	1.6476e-05	0.00287014	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287846	GAAGAGGTATTTGTA[A/G]AGAAAATGGAGTTCT	25897
rs770237677	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100300354	TTACTGAGAATTCAA[A/G]AGCAACAAAATCAGC	25897
rs770259411	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100309574	CACCAGGAGGACAGG[A/G]CTTGGGGCGGATCCC	25897
rs770282256	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100303124	TAACAAACTACCACA[A/G]ACTGGTTGGCTTAAG	25897
rs770287890	snp	C/T	1.64743e-05	0.00287	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287923	ATCCACCCCGCCATT[C/T]AGCTCCCTTGATTTA	25897
rs770327363	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100307147	AAAGATCATAAGCTT[A/C]TTAGTTCAGTACAAA	25897
rs770359833	snp	C/T	3.29755e-05	0.00406038	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259167	CACTGCCATCATCCA[C/T]ACTACTGCTTCCACT	25897
rs770369694	in-del	-/TTTAT			intron-variant	RNF19A	GRCh38.p7	8:100273768	AGCATTATTAGTATC[-/TTTAT]TTTATTATTATCATC	25897
rs770405294	snp	A/C/G			intron-variant	RNF19A	GRCh38.p7	8:100328083	TGCATTATGGGAGGC[A/C/G]AGATGAAAGGGCAGG	25897
rs770449613	in-del	-/A	1.80273e-05	0.00300222	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258512	AGTTCAACCAGCTCC[-/A]AACACGGTTGTACAG	25897
rs770482112	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258543	TGGTAATTATTCTGC[A/G]GCATTTATGGGCCTA	25897
rs770496127	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272686	GCACACACCACTAGA[A/G]ATGCACACCACCACG	25897
rs770534533	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100299588	AACATGGTGAAACAC[G/T]GTCTCTACTAGAAAT	25897
rs770630944	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100294184	ATTGTGGATATCTTA[C/T]AGAGGCTCTGTAGTC	25897
rs770676228	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100318456	TCAATTTTGAAACAA[A/G]GCAAATAAAAAATGT	25897
rs770688162	snp	C/G/T	6.59048e-05	0.00574009	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287610	CACTTAATATCAAGC[C/G/T]AATATCATGGGGATT	25897
rs770709090	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100331244	AGAATCCAAGTGGCC[A/G]TCCTTTTGAACCTTG	25897
rs770720767	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100295924	TACTAAAAAATCACA[C/T]TTAAATGTTATTTTT	25897
rs770720803	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100280987	TAATAAGTGTTATTT[C/G]GAAAAAGAACAGGCT	25897
rs770731647	in-del	-/AATT			intron-variant	RNF19A	GRCh38.p7	8:100271650	AAAATCACACATGAG[-/AATT]AATACCACAAGCAAT	25897
rs770737012	snp	C/G	1.64746e-05	0.00287002	missense, intron-variant	RNF19A	GRCh38.p7	8:100261711	CACCAACACTTCCCT[C/G]CCCTATGCTTGGGTT	25897
rs770741186	snp	G/T	1.6476e-05	0.00287014	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287801	ATGAAGTCTCCAATT[G/T]GTTTGCTGATGGAAG	25897
rs770790539	snp	A/G	3.44098e-05	0.00414774	intron-variant	RNF19A	GRCh38.p7	8:100263994	CCCACTACTTACACT[A/G]TTAATAAGCACATTT	25897
rs770801186	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100332297	GTGGTAATTTCCCCC[A/T]TGTTGTTCTCATGAT	25897
rs770805781	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100320922	TGTGCAATAGCATCA[C/T]GTGTAAAAATGTATA	25897
rs770839826	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272755	CACCATGTTGCCCAG[A/G]CTGTTGAAGTTTTAG	25897
rs770935015	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100306065	CTTATGGCTCACTTC[A/T]ACCAAAGTCTCTTCA	25897
rs770977351	snp	C/T	1.65924e-05	0.00288027	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269989	ATATAAGCAGCACAT[C/T]GTGGACATGGCTTTA	25897
rs771068846	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293692	AAGTATTTTTTACCA[C/T]ACTGTCTCTCTCTCT	25897
rs771082333	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100276370	CCATTTATATATTTT[G/T]GAAATGTCAAATAGA	25897
rs771094017	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310615	GAGGAAATGTCCTTT[C/G]CCAGAGGACGGCAGC	25897
rs771125441	in-del	-/A	1.65583e-05	0.00287731	intron-variant	RNF19A	GRCh38.p7	8:100264644	CATAAAATTGTAGGT[-/A]ATTAGTACTTTTCAG	25897
rs771127511	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100322746	AGATGTCATTGTAGG[G/T]TTACTAACTGGCCTA	25897
rs771151438	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307461	CAACAACAAACTATA[C/T]GTGTTGGAGAAGGGG	25897
rs771205027	snp	C/T	1.64855e-05	0.00287097	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259949	GACTGTGCCAGATTC[C/T]CCACTTAGACTGTAC	25897
rs771223618	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100324067	GAGGGAAAAACTGAA[C/T]AATTACTACAGAGCT	25897
rs771247090	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100266684	CCCAGCTGATTATTT[A/C]GTTTTTTGTAGAGAC	25897
rs771262422	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100260357	TCATTAAACATGACA[C/G]ACCAATGAATCCAAA	25897
rs771282649	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100264896	CATAGAAGTTCGTAG[C/G]TGAGTATCTTAGTTC	25897
rs771346642	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100316140	AAAGCTGCAGACCTT[C/T]GCGGTGAGTGTTACA	25897
rs771390660	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287944	CCTTGATTTACGTTT[A/G]TTATCTTTTTTCCTC	25897
rs771401953	snp	G/T	1.64942e-05	0.00287173	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264672	CAGCATTTTCTTACC[G/T]ACAGTCACTGCAGCT	25897
rs771461632	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100296252	TGTGACTACAGGCAC[A/G]TGCCACCATGCCTGG	25897
rs771494847	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100285146	AAGATTTTCTCTACA[A/G]TACTTACCTAGGAGT	25897
rs771549899	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100283096	TCCTTGGGAGGCTCA[A/G]AGACAATAAATCATT	25897
rs771601092	snp	A/C	3.29478e-05	0.00405867	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287914	TGCAATTCCATCCAC[A/C]CCGCCATTTAGCTCC	25897
rs771612288	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100333828	GTCTGTAAACAATAA[C/G]AACAAAAACCGAAAA	25897
rs771612291	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100316104	TTCTGGTGGGTTCGT[-/G]GGTCTCGCTGGCTCA	25897
rs771678977	snp	A/G	1.64754e-05	0.00287009	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287830	AGTTAATCCATTGTC[A/G]GAAGAGGTATTTGTA	25897
rs771699358	snp	A/C/G			intron-variant	RNF19A	GRCh38.p7	8:100328353	AATTATCAAATCCAA[A/C/G]AGACAAAGTGAACTT	25897
rs771719271	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100272913	CTCTGTCACCCAGGC[G/T]GGAGTGCAGTGGCAC	25897
rs771734211	snp	A/G	6.74479e-05	0.00580684	intron-variant	RNF19A	GRCh38.p7	8:100264023	TTTCTTCCTTTGCTT[A/G]AAGGACTTACCTACA	25897
rs771735905	in-del	-/TTTTTTTTTTTTT			intron-variant	RNF19A	GRCh38.p7	8:100313902	GAGAAAGAGAACTAC[-/TTTTTTTTTTTTT]TTTTTTTTTGAGACA	25897
rs771769211	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100284232	GATAGGGACTCAAAA[C/T]CAGGTATTTACAGCT	25897
rs771788330	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100294145	TTTTTTACATGCCTT[A/G]TAACTGCTTATTATA	25897
rs771789169	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316164	TGTTACAGCTCTTAA[A/G]ACGGCGTGTCTGGAG	25897
rs771841072	in-del	AAAAAAAAAAAAAAA/G			intron-variant	RNF19A	GRCh38.p7	8:100276724	TCACACCACTGTACC[AAAAAAAAAAAAAAA/G]AAAAAGAAAAAAAGG	25897
rs771867488	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100266956	AAAATGTATGTTGAA[C/T]ATAAAAAATTCAGCT	25897
rs771883804	snp	G/T	0.000198206	0.00995308	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258616	TGAGTGGTTGTTATT[G/T]GTTTCTTTTAGTGCA	25897
rs771913059	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100307242	CCTAAGATTTCCTAT[A/G]TAACCCGAGTAGAGA	25897
rs771935162	snp	C/G	1.65121e-05	0.00287329	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258736	AGCAGTTTGGGTAAC[C/G]ACAGAAATGCTACAC	25897
rs771942665	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100274528	TAAAGTACATGATTA[C/T]CTCAATACACTGCTG	25897
rs771943278	in-del	-/TTG			intron-variant	RNF19A	GRCh38.p7	8:100315652	TTCTTCGTCGTCTTG[-/TTG]TTGTTGTTGTTGTTG	25897
rs771947434	snp	A/C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289019	GAGCCGAGATTGCGC[A/C/T]GCTGCACTCCACCCT	25897
rs771976555	snp	A/G	1.67041e-05	0.00288994	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100270004	CGTGGACATGGCTTT[A/G]TATCATCAGCTATTG	25897
rs771987074	snp	A/G	1.64866e-05	0.00287106	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259966	CACTTAGACTGTACC[A/G]TTCTTTCTGTACATC	25897
rs772017560	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100265118	TTATTTTCAACACAG[G/T]TATGAGTTACATGGT	25897
rs772027591	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100308333	AAATTTTAAAAGTGT[G/T]TTTTTAGCATAATTT	25897
rs772029425	snp	A/G	1.66161e-05	0.00288232	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274963	AATACCTGCTGCTCC[A/G]GACTCTTGACTATAA	25897
rs772034717	snp	A/G			missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258758	ATGCTACACTGATGT[A/G]GGGAATTTTCCAGAC	25897
rs772172188	in-del	-/A	1.64757e-05	0.00287012	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287821	CTGATGGAAGTTAAT[-/A]CCATTGTCAGAAGAG	25897
rs772175232	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100262534	GTATAAAATAAGAGG[A/G]TGACAAGAGATGAGC	25897
rs772180834	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100279770	GACCTCAAGTGATCC[A/G]CCCACCTCAGCCTCC	25897
rs772187358	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100298814	AAAGCATTACTCATT[C/T]AATTTCTCCAATAAA	25897
rs772241749	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF19A	GRCh38.p7	8:100310120	CCCCTCCCGCAGCCC[C/T]CGCTTTCCCCTCCTC	25897
rs772252291	snp	C/G/T	0.000132402	0.00813546	intron-variant	RNF19A	GRCh38.p7	8:100261524	GAAAGCAGAACCAAA[C/G/T]CAAACCAAAACACAC	25897
rs772269196	in-del	-/CTTT			intron-variant	RNF19A	GRCh38.p7	8:100314621	CACACACCCTGCTAA[-/CTTT]CTTTCTCTTTGTAGG	25897
rs772345276	snp	A/T	1.64806e-05	0.00287054	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288062	TCTCGATCTGAACCC[A/T]TTTGCCGATGTAAAC	25897
rs772359857	in-del	-/TG			intron-variant	RNF19A	GRCh38.p7	8:100325344	TAGTTACAATGTAAC[-/TG]TGTAAATTTATAAAT	25897
rs772378148	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304894	AGTGTTTCAAAGGCA[C/T]AATTAACTTATACTA	25897
rs772393450	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100334690	ACGGTTTCATTGAGT[C/G]CCACTCCTTTCAAGA	25897
rs772403053	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303278	CATTCCTCGGCTTGC[A/G]GTTACATCACTCCAA	25897
rs772428727	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100313396	CAAGAAGAAGGCAAA[C/T]TAGTTAGGAGGTGGG	25897
rs772490530	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100290527	TTTCCTCCTATGGCT[C/G]ACCTCCTAATTAACA	25897
rs772543193	snp	A/T	1.65075e-05	0.00287289	intron-variant	RNF19A	GRCh38.p7	8:100264792	ATTGTGAATCTTGAA[A/T]TAATAAAAATAGGGG	25897
rs772550127	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100264419	AAAAGAGAGAGATGC[-/A]AACTTTTTTCTTTTG	25897
rs772574252	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291544	TCCCACCAATAAACA[C/T]CTAACCATAAACACT	25897
rs772588450	snp	A/G	1.64754e-05	0.00287009	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259082	GCTGTTGCTTCTTTG[A/G]ACCACTTGGTGGCAC	25897
rs772604428	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100325627	CTATATTTGCCATAT[C/T]TTGGCCCCATCCCAC	25897
rs772661494	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100335915	ACGTGACCCAAAGCA[A/G]CTATCCTATAGGTTG	25897
rs772732629	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100324096	CTGTGATTTTGAGAT[A/G]ACTTTGTTCAAAGAA	25897
rs772785578	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100280058	TGATTACTTATAATC[A/G]TAATTCCTCCACTTT	25897
rs772800661	snp	G/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336335	GTCTGCAGGCTGAAA[G/T]AGGTCAGGAGCTGCC	25897
rs772804531	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100325611	GGTCCTCAAGCCCAG[A/C]CTATATTTGCCATAT	25897
rs772867082	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100298778	AGTTATTACAAAAAG[C/T]AAGCTGCTGCAGAAA	25897
rs772867699	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100296967	GCCCACAGTAACCCA[C/T]CACATGTATTGAAAA	25897
rs772875972	snp	C/T	3.29935e-05	0.00406149	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275003	GAAGAACGTATAGTT[C/T]TCAAACGTAAGCTCT	25897
rs772909659	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100329617	ATGCAAACTAGCATG[A/C]ATCCAAAGACAGACA	25897
rs772925847	snp	C/T	1.64743e-05	0.00287	missense, intron-variant	RNF19A	GRCh38.p7	8:100261698	CTGCCAGTCAGCCCA[C/T]CAACACTTCCCTCCC	25897
rs772955950	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100293053	CCATCTAGATCCCTC[A/G]AGTGCAGTTCGCAAT	25897
rs772974040	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100284815	AAAATAATACTCCTG[C/T]ATCTACCACTGAAGT	25897
rs773043688	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100299411	ATTCAGTGTCAAAGT[C/G]AATTTTACCAAGTCT	25897
rs773063690	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285717	GGCTCACTGCAGCCT[C/T]GACCTCATGGGTTCA	25897
rs773067678	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100269573	CTAAATGATAAAATT[C/T]ATGTATGGGAAAATT	25897
rs773077180	snp	A/C	1.96976e-05	0.00313822	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288179	TGTTCTTGCATTCAC[A/C]TTAAGTCATGATGTA	25897
rs773148828	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100289273	TAAATATAAAGCTTC[C/T]AGGAGACAAAAGAGA	25897
rs773151756	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100271089	TACAAGTTTTATGGT[A/C]AAACTTTACCTGTGC	25897
rs773181650	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100331127	TCCCATATGGGTCAG[A/G]TGCTGGGCAATTCAA	25897
rs773195776	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100321162	TCTTCCTTCCACAAA[A/G]GATTTCTCTGTAGCA	25897
rs773270729	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100319366	ATTCATGTAGACCCT[A/G]TAAGAATAAATGTTA	25897
rs773360206	snp	A/G	1.69106e-05	0.00290775	intron-variant	RNF19A	GRCh38.p7	8:100268978	ATAATGTAAATAACT[A/G]CTGCAAAACACCACA	25897
rs773443343	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100262992	GGATGAAGGGAAGAA[C/G]AGATTTTAGAGCCAA	25897
rs773456523	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100322659	GGCCTGCCTTCCTCA[C/T]TAAGCTTAATCATTT	25897
rs773457217	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100333799	CTCCAGCCTGGGCAA[C/T]AGAGTGACACCCTGT	25897
rs773500030	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100275448	ACATGTGCAAGTTTG[A/T]TACATAGGTCTATTG	25897
rs773504557	snp	A/G	1.68261e-05	0.00290048	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259232	TCTACTTGCACCTCC[A/G]TACTGTTGCCTTCTC	25897
rs773590033	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100276261	ACTACCATCAATAAA[C/G]AAAGTATTGATGCAA	25897
rs773595690	snp	A/G	0.00051062	0.0159703	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287848	AGAGGTATTTGTAGA[A/G]AAAATGGAGTTCTTA	25897
rs773617903	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100280925	AAGTAAATTAAATAC[A/C]AGACACTTGCTTTAT	25897
rs773627654	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100302271	AAAGACTACTGAAGT[A/T]ATCTATGAGAAAGAT	25897
rs773646016	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285322	TTGGTGACAATCTAA[C/T]GTTTTCCCCCTCAAA	25897
rs773648955	snp	A/C/T	8.23722e-05	0.00641717	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287939	AGCTCCCTTGATTTA[A/C/T]GTTTGTTATCTTTTT	25897
rs773650054	in-del	-/AA			intron-variant	RNF19A	GRCh38.p7	8:100307264	GAGTAGAGAAGATAT[-/AA]GTGAGCAATTCAGAT	25897
rs773654890	snp	C/T	1.65018e-05	0.00287239	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264078	ATATCATTTTCATCA[C/T]CAAATTCAATCCTAA	25897
rs773657102	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100315247	GAGCCAAGATCACAC[A/C]ACTGCACTCCAGCCT	25897
rs773691924	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100282352	GAAATGCTTAAAGTT[C/T]ATTACACTGTCAGAA	25897
rs773694539	snp	A/C	2.13646e-05	0.00326831	intron-variant	RNF19A	GRCh38.p7	8:100259829	TTAAAAAATACTTTC[A/C]ATTTTTTAACAGTTT	25897
rs773822737	snp	A/G	1.65556e-05	0.00287707	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258610	CTGATGTGAGTGGTT[A/G]TTATTTGTTTCTTTT	25897
rs773944931	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303333	TTCCTCCTTTTCTGC[A/G]CGTCGTCTTCTCTGT	25897
rs773970283	snp	A/T	1.72686e-05	0.00293837	intron-variant	RNF19A	GRCh38.p7	8:100275209	GACATAAAACAAGAG[A/T]TACTCATTTCAAAAA	25897
rs774024016	in-del	-/CTC			intron-variant	RNF19A	GRCh38.p7	8:100286594	TCTGAAAATTCACTA[-/CTC]AAGAAACTTTTAAAT	25897
rs774080102	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100281014	GGCTCAATAGAAGGT[A/C]ATGGAAATAACTGAA	25897
rs774091538	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272797	TCAAGCAATCTGGCC[A/G]CTTTGGCCTCCCAAA	25897
rs774091574	in-del	-/A	1.71355e-05	0.00292702	intron-variant	RNF19A	GRCh38.p7	8:100264198	GGAACACCGATACCT[-/A]AAGAGAAATTAAATC	25897
rs774101615	snp	C/T	1.71399e-05	0.0029274	intron-variant	RNF19A	GRCh38.p7	8:100268995	TGCAAAACACCACAA[C/T]AACAAATTAGTGCAC	25897
rs774157471	snp	G/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100288829	ACTTTGGGAGGCCAG[G/T]ATGGGCGGATCACAA	25897
rs774167981	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100282976	TACCCAAATGTATAT[A/G]AGTTATGTTAGTAGC	25897
rs774189174	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100271403	TTATGCCTGATACAA[C/T]ACGTGGTATACTAAA	25897
rs774274737	snp	A/C	1.71935e-05	0.00293197	intron-variant	RNF19A	GRCh38.p7	8:100263997	ACTACTTACACTGTT[A/C]ATAAGCACATTTTCT	25897
rs774287856	snp	A/G	1.73607e-05	0.00294619	intron-variant	RNF19A	GRCh38.p7	8:100259254	TGCCTTCTCTGAAAT[A/G]TAAGAGTAACAAATA	25897
rs774297723	in-del	-/CAC			cds-indel, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264718	TTACAGACAACGTTA[-/CAC]CACCACCTGCTATGG	25897
rs774298286	snp	C/T			downstream-variant-500B	RNF19A	GRCh38.p7	8:100256807	TATATTTACTCAAGT[C/T]AAATTCAACCAATTT	25897
rs774303950	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100308938	TTTATATCTCCAAGG[A/G]TCAATGGGAAAAAAT	25897
rs774326075	snp	C/T	1.654e-05	0.00287571	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258611	TGATGTGAGTGGTTG[C/T]TATTTGTTTCTTTTA	25897
rs774372302	in-del	-/AA	1.7628e-05	0.00296878	intron-variant	RNF19A	GRCh38.p7	8:100259265	AAATATAAGAGTAAC[-/AA]ATACAAACATAATTG	25897
rs774383536	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280109	AAGAAATACAGTGAA[C/T]TGGCCAGTCATTAAG	25897
rs774486622	snp	C/T	1.66424e-05	0.0028846	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269997	AGCACATCGTGGACA[C/T]GGCTTTATATCATCA	25897
rs774535616	snp	C/T	1.66879e-05	0.00288855	splice-donor-variant	RNF19A	GRCh38.p7	8:100259853	ACAGTTTTTTCCTTA[C/T]TTGTCCAATGGGATG	25897
rs774579617	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100324075	AACTGAACAATTACT[A/T]CAGAGCTGTGATTTT	25897
rs774588449	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310651	GTGCGTCTGCAGCCG[C/T]CCTCTTAGTGCACCT	25897
rs774604135	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100319528	ACCTATCTGGTTCAC[-/T]TTTTTTTTTTTTTTT	25897
rs774652364	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100323206	GTTATTTTAAGATGA[G/T]GGGATATAGGACTCA	25897
rs774655073	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100260452	ATTTATATATATTTT[C/T]AGAGACAGGGTCTCG	25897
rs774712862	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316141	AAGCTGCAGACCTTC[A/G]CGGTGAGTGTTACAG	25897
rs774716880	snp	C/T	4.94613e-05	0.00497275	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264683	TACCTACAGTCACTG[C/T]AGCTACTACTGGAGA	25897
rs774769049	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100290502	TAATGTGCCTTTTTC[C/T]ATGTGTTTTTTTCCT	25897
rs774770130	snp	C/T	1.64977e-05	0.00287203	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264785	CATAGCGATTGTGAA[C/T]CTTGAATTAATAAAA	25897
rs774770215	snp	G/T	0.000247678	0.0111255	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258788	CGGTCATTTTCTACC[G/T]CAGGAAGAATGTTAA	25897
rs774798521	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303270	ACTATAAGCATTCCT[C/T]GGCTTGCGGTTACAT	25897
rs774803343	snp	A/G	1.64792e-05	0.00287042	stop-gained, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288051	AGGACTGAAGATCTC[A/G]ATCTGAACCCATTTG	25897
rs774822715	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100266694	TATTTAGTTTTTTGT[A/G]GAGACAAGGTGTCAC	25897
rs774832158	snp	A/C	1.64754e-05	0.00287009	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287833	TAATCCATTGTCAGA[A/C]GAGGTATTTGTAGAG	25897
rs774885656	snp	C/T	1.65419e-05	0.00287588	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264054	GCTGTGTTAGTTCCA[C/T]CAACATTTATATCAT	25897
rs774950734	in-del	-/AT			intron-variant	RNF19A	GRCh38.p7	8:100320190	AAATTCACAAATAAC[-/AT]ATTCTATTGTTTTAT	25897
rs774957250	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316212	TGGGCTTGTGGTCTC[A/G]CTGGCTCAGGAGTGA	25897
rs774969823	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100333897	CCTGTTCCCTACAGC[A/G]TGATGTTTAAATTAT	25897
rs774974576	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257220	GGACCTGGTAGGGAA[A/G]AGTGATGGAAGAAGA	25897
rs775045006	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF19A	GRCh38.p7	8:100303337	TCCTTTTCTGCGCGT[C/T]GTCTTCTCTGTAATG	25897
rs775052794	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100283318	AGGCAGAGGGTAATC[A/C]GATATTTTTATTCAA	25897
rs775057861	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100334594	TCCCTTTCTTGTGCC[C/G]CACCTCCGAGCTCCA	25897
rs775060795	snp	C/T	6.59e-05	0.00573983	missense, intron-variant	RNF19A	GRCh38.p7	8:100261720	TTCCCTCCCCTATGC[C/T]TGGGTTGTGTCTTGC	25897
rs775145015	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100274733	TTTGGCTATCAGTTA[C/T]ATAAATCATCACAAC	25897
rs775216839	in-del	-/CT	1.64746e-05	0.00287002	frameshift-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258932	GAAGGCATACTGTCA[-/CT]GAGGGATGGAGCCTC	25897
rs775217409	snp	C/G	1.64966e-05	0.00287194	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258627	TATTTGTTTCTTTTA[C/G]TGCATCGCCAAAATA	25897
rs775235182	snp	C/T			missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258789	GGTCATTTTCTACCT[C/T]AGGAAGAATGTTAAC	25897
rs775267515	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100307245	AAGATTTCCTATATA[A/G]CCCGAGTAGAGAAGA	25897
rs775287628	snp	G/T	1.67343e-05	0.00289255	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100270007	GGACATGGCTTTATA[G/T]CATCAGCTATTGGGA	25897
rs775331563	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100281188	CTAGGAGTGGATGGA[C/G]AGCAAGAAAGTGGGG	25897
rs775348038	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100332241	TCCCCATAATCCCCA[A/G]GTGTCGAGGGAGGGA	25897
rs775394096	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100268096	TTCTTGGATACCAAA[A/G]AAAATTTCTTTTTTT	25897
rs775412126	snp	C/T	1.65165e-05	0.00287367	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258752	ACAGAAATGCTACAC[C/T]GATGTGGGGAATTTT	25897
rs775431922	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100261382	GGATTACAGGCGTGA[A/G]CCACTGCACCTGGCC	25897
rs775435440	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100335014	TATACAGTTAAGCAA[A/T]CTGATTGAAGCAATT	25897
rs775555432	in-del	-/GGATTA			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303492	ATTTGCAGATTCTGG[-/GGATTA]GGACATGAACATATC	25897
rs775623542	in-del	-/AC			intron-variant	RNF19A	GRCh38.p7	8:100325768	GTGAGTATGTATTAC[-/AC]ACACACACACACACA	25897
rs775625802	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100295126	GATGATATCTTCTCC[A/C]AAGAGTAACATGAAT	25897
rs775659754	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100329897	TTCTCATGTATCCCA[C/T]ACATTTGCACAAATG	25897
rs775711924	snp	C/T	6.6107e-05	0.00574884	intron-variant	RNF19A	GRCh38.p7	8:100264802	TTGAATTAATAAAAA[C/T]AGGGGTGGGGGATTA	25897
rs775722817	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100297974	TTCAGCCTCTGAAAC[G/T]TACATTAACTATGTG	25897
rs775727648	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100262750	GATACAGCAGTTAAG[A/G]GGCTATTACAATAGC	25897
rs775744984	snp	A/C	3.295e-05	0.00405881	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287962	ATCTTTTTTCCTCCG[A/C]AACAGGGAGCCTATT	25897
rs775747518	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100331268	AACCTTGATTTCACA[G/T]AATGTAGAAAAGCCA	25897
rs775766964	snp	C/T	3.29484e-05	0.00405871	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258982	GCTTTGTTGTTCTAA[C/T]AACTGTGCATCCATG	25897
rs775799998	snp	C/T	1.64808e-05	0.00287057	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288064	TCGATCTGAACCCAT[C/T]TGCCGATGTAAACTC	25897
rs775840813	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100335931	CTATCCTATAGGTTG[A/G]CCGCTTTCTATACTA	25897
rs775896373	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100312726	GCCAGGAGTTTGATA[A/C]CAGCCGGGACAACAT	25897
rs775905447	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100323697	CCAAAATGGCTAATT[C/G]AAAGTTTGTGTGATA	25897
rs775930325	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100325282	CAGAGAACTTAAGAG[A/C]CTGAAGGGTTTTTGC	25897
rs775936133	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304915	ACTTATACTAATCCA[A/G]TGAAAAAGATGATGA	25897
rs775937773	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100291548	ACCAATAAACATCTA[A/G]CCATAAACACTTCAG	25897
rs775937872	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100276625	CCGGGAGTGGTGGCA[C/T]ACACCTTTAATCCCA	25897
rs775958531	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100334715	TCAAGACCCAGCCCC[A/G]CTGGCGTGCACCCAT	25897
rs775972917	snp	A/G	1.64849e-05	0.00287092	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268836	TGCAGGAATAGCAAT[A/G]CCAGCTATTAAAGCG	25897
rs776016119	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100271156	TAGGACCAAAGATGC[-/T]TTTTTTTTTTTTTTA	25897
rs776024031	snp	C/T	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259087	TGCTTCTTTGGACCA[C/T]TTGGTGGCACTAGAT	25897
rs776042627	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100324156	ATTTATTTTTTACAG[C/T]GGAGGAAGCCCAATC	25897
rs776096170	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100305110	CCAGCAAATTTTTGT[A/G]TTTTTTAGTAGAGGC	25897
rs776117698	snp	G/T	3.3089e-05	0.00406736	intron-variant	RNF19A	GRCh38.p7	8:100264647	AAAATTGTAGGTAAT[G/T]AGTACTTTTCAGCAT	25897
rs776190446	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291657	CAAAAAGTTTGCATA[C/T]ACAGAAAACACTTAC	25897
rs776207382	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310839	AATTACTTTAATCCA[C/G]CTTTATTTGTTCCTT	25897
rs776211866	snp	A/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303573	TTTTTGCTAAGGACA[A/T]CAGTAAGGTATGCTA	25897
rs776270381	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100335579	AAATTACTCCAAAGT[C/T]TACTGTACACATCAC	25897
rs776282911	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100318307	GTCTCCTTCCGGTCT[A/G]TGTATAAGATTTAAA	25897
rs776300859	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310575	GGCCGAGGGAGAGAA[C/G]TGCCGGGATGTTGCA	25897
rs776310282	snp	C/G	8.23676e-05	0.00641693	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258942	TGTCACTGAGGGATG[C/G]AGCCTCAAATTCACT	25897
rs776311031	snp	G/T	1.66599e-05	0.00288611	intron-variant	RNF19A	GRCh38.p7	8:100275169	CAGCATATCTTGAAA[G/T]AACAAGAAAAATGAT	25897
rs776434417	snp	A/C	3.29848e-05	0.00406095	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259997	TGCTTGTACTTCCAA[A/C]CTTAAAGGGGGGTAT	25897
rs776454129	snp	C/T	1.65263e-05	0.00287452	missense, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100274983	CTTGACTATAACTAA[C/T]GGATGAAGAACGTAT	25897
rs776486622	snp	A/G	1.65209e-05	0.00287405	intron-variant	RNF19A	GRCh38.p7	8:100261538	ACCAAACCAAAACAC[A/G]CACCTGTTAAAACAG	25897
rs776489892	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100322870	CATTTATTAAGTTCA[C/T]TGTCTTCAGTGGGAG	25897
rs776514072	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100297783	TCTGTTACAGATACA[A/G]TTATCTATCTTACTC	25897
rs776514191	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283666	GTAAGGACAGTATTT[C/T]TCAAGGTGTGTTAAA	25897
rs776563495	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100312742	CAGCCGGGACAACAT[C/G]ATGAAACCTCATCTC	25897
rs776608201	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100331393	GTAATCCCAGTACTT[C/T]GGGAGGTCAAGGTGG	25897
rs776678128	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100328574	CCTCCCGGGTTCAGG[C/T]GATTCTCTTGCCTCA	25897
rs776748241	in-del	-/TTC			intron-variant	RNF19A	GRCh38.p7	8:100296098	GCATTATTCTTTTTT[-/TTC]TTTTTTTCCTTTTTT	25897
rs776765940	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316344	TTCCACAGTGTGGAA[A/G]GGGACCCCAGTGGGT	25897
rs776827526	in-del	-/A	0.000107468	0.00732956	utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288199	TCATGATGTAAGAAT[-/A]ATCCTACTTGGTTCC	25897
rs776829432	snp	A/G	1.64825e-05	0.00287071	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288070	TGAACCCATTTGCCG[A/G]TGTAAACTCATGTCT	25897
rs776879331	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100332613	GATAAGACAAATGGT[C/G]TTATCAGCAATGTAT	25897
rs776881265	snp	C/G/T	7.04168e-05	0.00593331	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288156	ATTTAGAGATAAAAC[C/G/T]TATTTCTTGTTCTTG	25897
rs776913753	in-del	-/TGCAGCTACTACTGGAGACACGAT	1.64893e-05	0.0028713	cds-indel, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264681	CTTACCTACAGTCAC[-/TGCAGCTACTACTGGAGACACGAT]TACAGACAACGTTAC	25897
rs776934212	snp	C/T	9.88989e-05	0.00703134	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268853	CAGCTATTAAAGCGA[C/T]TCCGACAGGAGCACC	25897
rs776945918	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100276042	GGAATACCTTTCTCC[A/G]AGTTAATATTTCTGA	25897
rs776967746	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100278933	GGCAAGAAAACAGAG[A/G]AAACCGTGGACCTAA	25897
rs777002769	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100300248	ACTGTATAAGGAAAG[A/T]AAAGGGAGTATTTTC	25897
rs777057805	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100261439	TTTGAACCTTGACAT[A/G]GTAGGGTTATATATA	25897
rs777059698	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100279872	GTTTTGCCATGTTAG[C/T]CAGGCTGGTCTCGAA	25897
rs777070551	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100313725	AGAGTGGAAGTAGGG[A/G]GACCAGTTAAGAGGC	25897
rs777139065	snp	A/G	1.64773e-05	0.00287026	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287631	CATGGGGATTAAACC[A/G]TTCAGTACATTCTGG	25897
rs777188541	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303807	GCTGGGTGTGGTGGC[A/G]GGTGCCTGTAATCCC	25897
rs777249891	snp	A/G	1.64868e-05	0.00287109	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268830	AATCATTGCAGGAAT[A/G]GCAATGCCAGCTATT	25897
rs777276510	snp	C/T			downstream-variant-500B	RNF19A	GRCh38.p7	8:100257010	CTACCACATGGCCAA[C/T]GAATATTCTCATTCT	25897
rs777304914	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259072	TTTTTTCCCTGCTGT[C/T]GCTTCTTTGGACCAC	25897
rs777332608	in-del	-/G			intron-variant	RNF19A	GRCh38.p7	8:100326665	TTCAAGTTTCTCTAT[-/G]CTTATTTCCTTCCCA	25897
rs777357110	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100333483	ATATTAGAGGCAAGA[C/T]TCAAGATTGCTTATA	25897
rs777383939	snp	G/T	1.65081e-05	0.00287293	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100268922	GGCTCCAGGGTTTCT[G/T]CCCCCAAAAAGTACA	25897
rs777402291	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100262466	GAGAACTGCCAGTTT[A/C]AAAGCCTAGAAGTAG	25897
rs777483357	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258253	TATATTGATTATATA[A/C]ATTAAGACCAATTTC	25897
rs777530863	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100307092	TTACTTTGGGCTTTT[A/G]CCCAAGGTGGCCTAA	25897
rs777593281	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100301219	AACATTTCCTTCACC[A/G]CAGAAAGTTCTATTG	25897
rs777594073	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280566	CTTACTGAATTTATA[C/T]AAATTCCGAAGAAAA	25897
rs777619032	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100307895	TGTGTTAGGCAGAAA[A/G]TAAGTTTCAGTCAAG	25897
rs777659943	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100277783	CAGATAAAGAAAAAA[G/T]ACCCTATTTTTTTTA	25897
rs777661993	in-del	-/AAC			intron-variant	RNF19A	GRCh38.p7	8:100298211	GTTAAAAAAAAAAAA[-/AAC]ACTTATTACACATTA	25897
rs777683884	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100263618	AGGCAGTCTATGAAG[A/G]CTTTTTTATTCTTCT	25897
rs777712784	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100274365	CCCATACCTACAAAT[C/T]AACACTAATACTACT	25897
rs777714797	in-del	-/C			intron-variant	RNF19A	GRCh38.p7	8:100295322	ACTTTTGACAGCACT[-/C]CTATTTTTCGTAGTT	25897
rs777718949	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100305682	TAGCAAATACTTATT[C/T]GACATCTTTTATTGT	25897
rs777763839	snp	A/G	1.6477e-05	0.00287024	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287788	CAAAGGGCACTCTAT[A/G]AAGTCTCCAATTTGT	25897
rs777781418	snp	A/C	1.6495e-05	0.0028718	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258700	AGCAATATGATTCAA[A/C]TGTGAAACTTCTGAA	25897
rs777795565	snp	A/G	1.65509e-05	0.00287666	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269982	CTTTATTATATAAGC[A/G]GCACATCGTGGACAT	25897
rs777856945	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100295806	TTTTATAAATCTGAA[A/T]CATATCATTAAGAGA	25897
rs777884228	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100268264	ATATAATTCATCAAT[A/T]AGAGGCCAGTGGTAG	25897
rs777891370	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100303042	CACATGATATAAAAC[A/G]ACGATAATTAGAGAT	25897
rs777983081	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100290377	AAAGTGCTGGGATTA[C/T]AGACGTCAGCCACAG	25897
rs778048579	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100263775	TTATTTATAATGTTT[C/G]AGGCAAAATTTAAGA	25897
rs778083055	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100282667	CTGGATAAAATCAAA[C/G]TAGGATCTGTGATCT	25897
rs778092928	in-del	-/AACCA	0.00251839	0.0353956	intron-variant	RNF19A	GRCh38.p7	8:100261516	GTTACCAGAAAGCAG[-/AACCA]AACCAAACCAAACCA	25897
rs778113050	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100327139	TTTAATCTTAGCCTC[A/G]CTAACAAATGTAAAG	25897
rs778170832	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100266589	GATCACAGCTCACTG[C/T]AGCCTCAACCTCACG	25897
rs778180954	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100309639	CCCGCGCCTGGGCCG[C/G]GTAGGGGACCCGGAG	25897
rs778206984	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100328167	TTCTTTGAGTCAGGG[A/G]AGACTCCACCTTCTG	25897
rs778276238	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100295761	GATGTATTTCTACCC[A/T]AGCTAATTTTGGCCC	25897
rs778296924	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100316078	TGGTCAGATGTGTTC[A/G]GAGTTTCTTCTTTCT	25897
rs778332942	in-del	-/GA			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311916	CCTAAAAATTAGAAG[-/GA]CTTTCTATTCTTCAC	25897
rs778362658	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100296013	TAGAAATGTCATTAT[C/T]TTCCTCTAATAAATT	25897
rs778365794	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100297205	ATGAAGACATTTAAT[A/G]CCCAATGTGAAAGAA	25897
rs778372315	snp	C/G	1.65427e-05	0.00287595	intron-variant	RNF19A	GRCh38.p7	8:100260042	TATATTTAATATCAG[C/G]ACTACTGTAATATGT	25897
rs778375467	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100283978	TGTGTGTTTCAAAGG[C/T]TTCAGTAAGCTTCAA	25897
rs778407195	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100323325	TTTTATCTGAATATT[G/T]TCCTTTTCCTTTCAC	25897
rs778456282	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100259778	TAGCCACTTTTCACT[A/G]GTAATTTGTCTAATG	25897
rs778479512	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100305859	CTTACCATTTTCAGG[G/T]GCAAATACCAATACG	25897
rs778560993	snp	A/T	1.64741e-05	0.00286998	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287899	TATACTTTCAATACT[A/T]GCAATTCCATCCACC	25897
rs778561719	snp	C/T	8.23764e-05	0.00641727	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287817	GTTTGCTGATGGAAG[C/T]TAATCCATTGTCAGA	25897
rs778687554	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100332459	GAGGCCTCCTTGGCC[A/G]TGCAGAACTGTGAGT	25897
rs778694458	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100328335	GGAGAGGTCAGCAGT[A/G]GAAATTATCAAATCC	25897
rs778739101	snp	C/T					GRCh38.p7	8:100290300	AGAGACAAGGTTTCA[C/T]CATGTTGGTCAGGCT	25897
rs778777134	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100333539	TATATCAAAATCAGA[A/G]AGAAATATGTCAAAG	25897
rs778810116	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293937	TTTTCAGTTCTATAA[C/T]ATCTATTGTTCTTTT	25897
rs778829608	in-del	-/A	1.64764e-05	0.00287018	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287817	TTTGCTGATGGAAGT[-/A]TAATCCATTGTCAGA	25897
rs778864975	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100322327	CTTCACCTTGTACTT[C/T]CATGGCACAAAACAA	25897
rs778891386	snp	A/G	1.75096e-05	0.0029588	intron-variant	RNF19A	GRCh38.p7	8:100264218	GAAATTAAATCAGTC[A/G]TTACAAACAACAACA	25897
rs778914330	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100267992	CTGTTAGTTCCCTTT[C/T]TGAAAATTGCTATCC	25897
rs778935718	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100274442	AAGTATAAAAAAACA[C/T]TTATGTTACAAAAGT	25897
rs778954738	snp	A/G	1.64784e-05	0.00287035	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264733	ACACCACCTGCTATG[A/G]CCAAATTCCGTTTGT	25897
rs779009778	snp	C/G	1.64779e-05	0.00287031	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258867	TTTTCATGCTTTCTA[C/G]GTCAGAACAACTAAA	25897
rs779014533	snp	A/G	1.78516e-05	0.00298755	intron-variant	RNF19A	GRCh38.p7	8:100274938	ATTTTATTAGAAAAA[A/G]TTAGACATAAATACC	25897
rs779067750	snp	A/G	1.64808e-05	0.00287057	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275113	ACAGCCCTCTCGCCC[A/G]CAAGTTAATTTTGGA	25897
rs779075751	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100270371	TGAATGGTAGTTCCC[A/G]GTTCCAGAACTTTTC	25897
rs779185300	snp	C/T	0.000115396	0.00759505	missense, intron-variant	RNF19A	GRCh38.p7	8:100261609	CTCCAGCTAGTGCCA[C/T]GGTGCTGGCCGTTTC	25897
rs779224139	snp	G/T	3.30207e-05	0.00406316	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288112	TAGAATTGAGACAGG[G/T]TCAGTGTTTACACAC	25897
rs779232463	snp	A/G			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336827	AGGCCGTCAACTGTC[A/G]CTTTTTATTGCTGTA	25897
rs779232640	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100325128	GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	25897
rs779248451	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100317820	AGCTTGCTCAGGACA[C/T]TCATGGCTTACACCT	25897
rs779268436	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100325358	CTGTGTAAATTTATA[A/G]ATTATAAAATTACAA	25897
rs779339916	in-del	-/A			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100303762	AACCTCGCCGCTTGT[-/A]AAAAAAAAAAAAAAA	25897
rs779415807	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100284083	ATGATTATCTGATTT[A/T]AAAAAAAAAAGCAAA	25897
rs779443886	snp	C/T			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100304736	ATTTATTGTTACTGA[C/T]TCCAATGTGGGAGGT	25897
rs779502580	snp	C/T	3.29549e-05	0.00405911	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288000	TTCTTTTTTTGGGTG[C/T]CTTTTTGACTGAAGG	25897
rs779507428	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100268344	TATTTATTAAAAGCA[A/G]TAATCCAAAAAAAAA	25897
rs779514346	in-del	-/TT			intron-variant	RNF19A	GRCh38.p7	8:100272875	TTCTAATTCTTCCTC[-/TT]GTTTTTGGAAACAGG	25897
rs779536957	in-del	-/A	1.70038e-05	0.00291575	intron-variant	RNF19A	GRCh38.p7	8:100275199	TTTAAAATGTGACAT[-/A]AAACAAGAGATACTC	25897
rs779570370	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100309249	ACACCATTTTGGTGT[G/T]ATGTGTAATTTTTGC	25897
rs779587880	in-del	-/TT			intron-variant	RNF19A	GRCh38.p7	8:100292439	CTATCATATGGGTGT[-/TT]GTGTGTGTGTGTGTG	25897
rs779599438	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100270299	AATCAAGGACAGCTC[C/T]AGGCAAATTGTGAAC	25897
rs779636826	snp	C/T	1.64743e-05	0.00287	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287916	CAATTCCATCCACCC[C/T]GCCATTTAGCTCCCT	25897
rs779692396	snp	C/T	1.89525e-05	0.00307829	intron-variant	RNF19A	GRCh38.p7	8:100264247	CAACAAAATAACTCA[C/T]AGAAACATGAGTTTT	25897
rs779703203	snp	A/G	1.64855e-05	0.00287097	synonymous-codon, nc-transcript-variant	RNF19A	GRCh38.p7	8:100264771	AACATCCTTGCCTTC[A/G]TAGCGATTGTGAATC	25897
rs779819358	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100285547	CAATTAAGTGACCAG[-/A]AGGTTTGTGTCCCTG	25897
rs779821340	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100318076	TGTGGTATAATACTT[C/T]GGGCCTACATTAAGG	25897
rs779840288	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100298741	TTTAATAATACTCAT[C/T]ACAAGTAATATTCAC	25897
rs779878520	in-del	-/T	1.65146e-05	0.0028735	intron-variant	RNF19A	GRCh38.p7	8:100261800	AAGTATGATTATCAA[-/T]TTTTCTCCTTCTTAA	25897
rs779899078	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100334352	TCCACACAGTGCTGA[A/G]CAGAGGGTAAGGCTC	25897
rs779916543	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100323518	TCACATTAACTGCAC[A/G]TATGCTAGCCAAGAA	25897
rs779999692	snp	A/C			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337817	TTGGTGATATTACCT[A/C]TCAGCACCTGGAGTT	25897
rs780004482	snp	A/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100310431	AGCGTCTCCTCCAAG[A/G]ACAGGTCGGGGTGGC	25897
rs780039339	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258905	AAATGACTAGAGTGA[A/G]AATCTGCTACAGAAG	25897
rs780061626	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100273615	ATAATAAAAGCCATT[C/T]CTGTCGTTTTTTAAT	25897
rs780071117	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100263127	GGTCTATGCATTATT[A/T]AATAGATGAGATTAG	25897
rs780072717	snp	C/T			missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259978	ACCGTTCTTTCTGTA[C/T]ATCTGCTTGTACTTC	25897
rs780078832	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100291209	CACCTCAAATAGATG[C/T]TCTAAGAATAATATG	25897
rs780079811	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100296525	AATGCTTAAAATAAC[A/T]GCTAATGCATGGACT	25897
rs780088628	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100326904	TAAGTGTTATCTTAT[A/G]CTTCTTTTCCTTTTG	25897
rs780093181	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100259044	CCTTTTTCCTCAGTT[C/T]ACCACTTTTTGATTT	25897
rs780102078	snp	G/T	1.64942e-05	0.00287173	synonymous-codon, intron-variant, nc-transcript-variant	RNF19A	GRCh38.p7	8:100275140	TGGACAGCTGGCACA[G/T]CCAAATGCTATCACA	25897
rs780103897	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100279791	CTCAGCCTCCCAAAG[A/T]GCTGGAATTACAAGT	25897
rs780106006	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293704	CCACACTGTCTCTCT[C/T]TCTCTTCCCACTCCT	25897
rs780113994	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100270548	TAAGCACTATAAAAA[C/T]AGCAAAACAGGTATC	25897
rs780155134	snp	A/G	1.65266e-05	0.00287455	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287553	CTGCAACAAGCCACC[A/G]TCTAAGCATAAATTC	25897
rs780169024	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100277763	CAGCTTATTCATCGC[A/C]GTCCCAGATAAAGAA	25897
rs780172153	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100263999	TACTTACACTGTTAA[G/T]AAGCACATTTTCTTC	25897
rs780195444	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100280668	TTTGTCTAGTAGTTT[C/T]TTCTCACACTAACAC	25897
rs780198270	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100326002	TACAAATCTATGTGC[C/T]ACAAAGCTATATGCT	25897
rs780211698	snp	C/G	1.64849e-05	0.00287092	missense, intron-variant	RNF19A	GRCh38.p7	8:100261624	TGGTGCTGGCCGTTT[C/G]ACTCAGGTTGTCTCG	25897
rs780253317	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100286431	CTAATTCATAAAATA[C/T]TAATTAGGTAATTTT	25897
rs780373357	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100313417	AGGAGGTGGGGAAGA[C/T]GGAGGAACAGCAGAC	25897
rs780463238	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100314716	GCTCATTTCTATCAA[C/T]TCTCACTGGTCCTGA	25897
rs780475774	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257093	TTACATTTATTTAAC[A/G]TATGCAGTTTACACA	25897
rs780534870	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100270699	ATGAACGTTATAAAC[C/G]ATGGAAAACAGTTTC	25897
rs780563239	snp	A/G	1.71009e-05	0.00292406	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288148	TTCATTATATTTAGA[A/G]ATAAAACCTATTTCT	25897
rs780589320	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100292891	TACATATTTACTTTC[C/T]GGTACTTTTCAATCT	25897
rs780624735	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100272027	CATATTAAGAAAAAA[C/T]AACAGGTTACAAAAC	25897
rs780634507	in-del	-/AT			intron-variant	RNF19A	GRCh38.p7	8:100286631	GATTTGATTCAGGTA[-/AT]GAGTCTTGAAGTTGT	25897
rs780673010	snp	C/G	1.64795e-05	0.00287045	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288040	AGATGAAGCAGAGGA[C/G]TGAAGATCTCGATCT	25897
rs780673099	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100285567	TTGTGTCCCTGAATT[C/T]ACTGTCTTAATATCT	25897
rs780693431	in-del	-/AC	1.65057e-05	0.00287273	frameshift-variant, intron-variant	RNF19A	GRCh38.p7	8:100261550	CACACACCTGTTAAA[-/AC]AGTTTACCATGGCAC	25897
rs780734226	snp	G/T	1.64963e-05	0.00287192	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100288102	AAATGCTTGTTAGAA[G/T]TGAGACAGGGTCAGT	25897
rs780755336	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100290188	GAAGCAATCTCGGCT[C/G]ACTGCAGCCTCCATC	25897
rs780781380	in-del	-/T	1.64743e-05	0.00287	utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258547	AATTATTCTGCAGCA[-/T]TTATGGGCCTAAATT	25897
rs780928185	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100272104	GGTAAGGGGACAGAG[A/G]CAGGAGTGGAGAGCC	25897
rs781029142	snp	G/T			intron-variant	RNF19A	GRCh38.p7	8:100305809	CACATAGTCTCATTT[G/T]TGATTATGCATTAGA	25897
rs781044203	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100313019	ACCACTGCCAGGGCC[C/T]CATCATTTCCCACTG	25897
rs781115613	snp	C/T	6.59109e-05	0.0057403	missense, utr-variant-5-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100287762	CTGTCTTTAGAATGC[C/T]GCAAAAGGCACAAAG	25897
rs781153247	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100298644	AGGTATTTCTTAAAC[A/T]GCTTCACAAACACGC	25897
rs781162494	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100299068	ATATCCAAAGGAAAA[C/G]AGACACATTTTGCTT	25897
rs781165373	snp	C/T	1.65244e-05	0.00287436	intron-variant	RNF19A	GRCh38.p7	8:100261803	GTATGATTATCAATT[C/T]TCTCCTTCTTAAATT	25897
rs781241206	snp	A/T			intron-variant	RNF19A	GRCh38.p7	8:100317156	AGCCCGGGTTCCCGC[A/T]CGCGCCTCTCCCTCC	25897
rs781275309	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100262338	GTACATGTCTGTGAG[C/T]CATTTTATATGATGT	25897
rs781297676	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100282357	GCTTAAAGTTTATTA[C/T]ACTGTCAGAAGACAT	25897
rs781306102	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100266472	TTTGAATAACTACAT[A/G]AAAAATTACGATCAG	25897
rs781321288	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100302880	CAAGTTAGGAGAAGA[A/C]AGAAACGATACAAGC	25897
rs781322228	snp	C/T	1.64768e-05	0.00287021	missense, intron-variant	RNF19A	GRCh38.p7	8:100261660	CTCCTATTCGATCCA[C/T]GTGGCTTCCACTTGC	25897
rs781323753	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100302677	TGAGGTCTGTAGCAT[C/T]CCAACATTAAGATGT	25897
rs781339153	snp	A/G	1.67832e-05	0.00289677	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100258590	GCAACTTTTAATTCC[A/G]TTGTCTGATGTGAGT	25897
rs781342641	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100315137	TCTAGGAGTTTTGTC[A/G]TGTGCCCAGGCATGG	25897
rs781408735	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100327091	TTTTGCTATGAAAAA[-/A]GTCCCACACATCTTT	25897
rs781474183	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF19A	GRCh38.p7	8:100257696	CAGAGAAGACATGGA[A/G]AACAACACAGCAAAA	25897
rs781488684	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100293903	CCATCCAGTGAAATT[C/T]TCATTTTAGATATTG	25897
rs781513383	snp	G/T	7.8882e-05	0.00627971	intron-variant	RNF19A	GRCh38.p7	8:100259810	TAGGAATTATTCCTT[G/T]AATTTAAAAAATACT	25897
rs781563855	snp	G/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100337169	ATCTCTGGTTCTGAG[G/T]AATCAAAACATACTG	25897
rs781574609	snp	C/G/T			intron-variant	RNF19A	GRCh38.p7	8:100280767	GCACGTTCTGTAATA[C/G/T]ATCAAGGAATTAAAT	25897
rs781619189	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100306439	TACTAGATAACATCA[A/G]TAGGATAAGACTACA	25897
rs781648049	snp	C/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100338116	CCCAAGTAGCTGGGA[C/T]TACAGGCACCCACTA	25897
rs781677545	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100307009	ATTCAACTACCATTT[C/T]GCTATGATGTGCTAG	25897
rs781711127	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100331225	TCTGAATCTCAGTTT[A/G]GAGAGAATCCAAGTG	25897
rs781722244	snp	C/T	1.65045e-05	0.00287263	missense, nc-transcript-variant	RNF19A	GRCh38.p7	8:100269947	GCACATGTCATGTGA[C/T]TGCAGCTCCCATCAT	25897
rs781748716	snp	C/T	1.71572e-05	0.00292888	intron-variant	RNF19A	GRCh38.p7	8:100270045	GAAATCTATTAAGTA[C/T]ATAAAACTGGTCTAA	25897
rs781754661	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100327057	GATTCTATGTGGATT[A/G]TCTTCCAGGTACTTT	25897
rs796085558	in-del	-/AG			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311739	AAAAAAAAAAAAAAA[-/AG]AAAAGAAAATAGATC	25897
rs796097395	snp	C/G			intron-variant	RNF19A	GRCh38.p7	8:100325946	ATGTCTGAACACTCA[C/G]AGAATTCAGGGTATA	25897
rs796339810	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100292785	ATTTTTTAATTTCTT[-/A]ATTTTTGAGACATTT	25897
rs796423888	in-del	-/CCA			intron-variant	RNF19A	GRCh38.p7	8:100267410	ATCTTGCTCTATCAC[-/CCA]CCAGGCTGGAGTGAA	25897
rs796462874	snp	A/G			intron-variant	RNF19A	GRCh38.p7	8:100271563	TGCATGCAATCTTTG[A/G]AACAAACTGAAAGGT	25897
rs796476877	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100322000	AAATTCTTTTTTTTT[-/T]CTTTATCAATACCCT	25897
rs796500964	snp	C/G			intron-variant, upstream-variant-2KB	RNF19A	GRCh38.p7	8:100311155	ATGGTCTTTCCGAAT[C/G]TACTTGGTATCTTTG	25897
rs796540852	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100279691	ACCATGCTTGGCTAA[-/T]TTTTTTTGTATCTTT	25897
rs796728529	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100308701	CTTTAAAAAAAAAAA[-/A]TGTGGAATGTAAAGA	25897
rs796740514	in-del	-/T			upstream-variant-2KB	RNF19A	GRCh38.p7	8:100336754	GTTTTTTTTTTTTTT[-/T]CTTCTTTGGAATTAT	25897
rs796741206	in-del	-/A			intron-variant	RNF19A	GRCh38.p7	8:100333090	GTATGGAAAAAAAAA[-/A]GAACAAACCTAGGTT	25897
rs796756419	in-del	-/T			intron-variant	RNF19A	GRCh38.p7	8:100294614	AGCCAGTAAGACTCT[-/T]GATTTTCTGCTTGAC	25897
rs796766346	snp	A/C			intron-variant	RNF19A	GRCh38.p7	8:100268222	CCATTAACCCTTAAC[A/C]AAAGAACTATTTGCT	25897
rs796774658	in-del	-/AC			intron-variant	RNF19A	GRCh38.p7	8:100325767	GTGTGAGTATGTATT[-/AC]ACACACACACACACA	25897
rs796858384	in-del	-/TC			intron-variant	RNF19A	GRCh38.p7	8:100319311	GGATGAAAGTTTTTT[-/TC]TTTTTTAACACAAAA	25897
rs796894583	in-del	-/CCAGCAGCGCTGCCCGGCTACTCTGAGTGCGGGGCCTGC			intron-variant	RNF19A	GRCh38.p7	8:100317042	CCTCATTGCCCGGGA[lengthTooLong]CAAGCCCACGCCCAC	25897
rs796981275	in-del	-/TCT			intron-variant	RNF19A	GRCh38.p7	8:100315647	TTTTCTTCTTCGTCG[-/TCT]TCTTGTTGTTGTTGT	25897
rs796999353	snp	C/T			intron-variant	RNF19A	GRCh38.p7	8:100294892	CAATACCTGGAACTG[C/T]AAGGTCTTCAACGAA	25897

Page 1 | 2