Variants in gene combination AMACR, C1QTNF3-AMACR with conflicting interpretations reported as "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: 7

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HGVS	dbSNP	gnomAD frequency
NM_014324.6(AMACR):c.602T>C (p.Leu201Ser)	rs2287939	0.73966
NM_014324.6(AMACR):c.25G>A (p.Val9Met)	rs3195676	0.42007
NM_014324.6(AMACR):c.524G>A (p.Gly175Asp)	rs10941112	0.38660
NM_014324.6(AMACR):c.717G>T (p.Gln239His)	rs34677	0.11264
NM_014324.6(AMACR):c.782T>C (p.Met261Thr)	rs3195678	0.01320
NM_014324.6(AMACR):c.837G>A (p.Thr279=)	rs35655488	0.00378
NM_014324.6(AMACR):c.438G>A (p.Pro146=)	rs140523570	0.00013

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