List of variants reported as likely benign for Dubin-Johnson syndrome by Illumina Laboratory Services, Illumina

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000392.5(ABCC2):c.4062C>T (p.Ala1354=)	rs17216275	0.01590
NM_000392.5(ABCC2):c.1058G>A (p.Arg353His)	rs7080681	0.01505
NM_000392.5(ABCC2):c.*259G>T	rs138578110	0.00931
NM_000392.5(ABCC2):c.842G>A (p.Ser281Asn)	rs56131651	0.00539
NM_000392.5(ABCC2):c.3107T>C (p.Ile1036Thr)	rs45441199	0.00494
NM_000392.5(ABCC2):c.3817A>G (p.Thr1273Ala)	rs8187699	0.00331
NM_000392.5(ABCC2):c.4509-9T>C	rs180717330	0.00294
NM_000392.5(ABCC2):c.1032-3C>T	rs139800035	0.00253
NM_000392.5(ABCC2):c.159A>G (p.Lys53=)	rs17222596	0.00191
NM_000392.5(ABCC2):c.2813G>A (p.Ser938Asn)	rs112339372	0.00158
NM_000392.5(ABCC2):c.2743C>T (p.Arg915Cys)	rs112758556	0.00150
NM_000392.5(ABCC2):c.2944A>G (p.Ile982Val)	rs17222554	0.00140
NM_000392.5(ABCC2):c.4313+11A>C	rs17222681	0.00107
NM_000392.5(ABCC2):c.2747+5G>A	rs138988852	0.00024
NM_000392.5(ABCC2):c.3500T>C (p.Val1167Ala)	rs140680467	0.00024
NM_000392.5(ABCC2):c.3542G>T (p.Arg1181Leu)	rs8187692

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