Variants in gene EGR2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000399.5(EGR2):c.1086A>C (p.Arg362=)	rs45602133	0.04462
NM_000399.5(EGR2):c.1399G>C (p.Ala467Pro)	rs146116229	0.00148
NM_000399.5(EGR2):c.192G>C (p.Met64Ile)	rs146631014	0.00024
NM_000399.5(EGR2):c.665T>C (p.Met222Thr)	rs530614586	0.00004
NM_000399.5(EGR2):c.1352G>T (p.Gly451Val)	rs138967272
NM_000399.5(EGR2):c.910GCC[7] (p.Ala309dup)	rs753747037

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