Variants in gene ABCC2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
NM_000392.5(ABCC2):c.-24C>T	rs717620	0.15338
NM_000392.5(ABCC2):c.4544G>A (p.Cys1515Tyr)	rs8187710	0.08637
NM_000392.5(ABCC2):c.3563T>A (p.Val1188Glu)	rs17222723	0.05531
NM_000392.5(ABCC2):c.1446C>G (p.Thr482=)	rs113646094	0.01182
NM_000392.5(ABCC2):c.3107T>C (p.Ile1036Thr)	rs45441199	0.00494
NM_000392.5(ABCC2):c.4527C>T (p.Asn1509=)	rs8187709	0.00269
NM_000392.5(ABCC2):c.3492C>T (p.Ser1164=)	rs144192700	0.00159
NM_000392.5(ABCC2):c.2073C>A (p.Val691=)	rs17222624	0.00155
NM_000392.5(ABCC2):c.3026T>C (p.Ile1009Thr)	rs57351269	0.00129
NM_000392.5(ABCC2):c.4495A>G (p.Met1499Val)	rs149200446	0.00078
NM_000392.5(ABCC2):c.2613A>G (p.Glu871=)	rs76302654	0.00056
NM_000392.5(ABCC2):c.2366C>T (p.Ser789Phe)	rs56220353	0.00017
NM_000392.5(ABCC2):c.3498C>T (p.Thr1166=)	rs564908429
NM_000392.5(ABCC2):c.3972C>T (p.Ile1324=)	rs3740066

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