Variants in gene MESP2 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001039958.2(MESP2):c.573G>A (p.Gly191=)	rs113097169	0.13255
NM_001039958.2(MESP2):c.185G>A (p.Arg62Gln)	rs566641514	0.00041
NM_001039958.2(MESP2):c.189C>G (p.Ala63=)	rs534821207
NM_001039958.2(MESP2):c.498C>A (p.Pro166=)	rs200336355
NM_001039958.2(MESP2):c.498C>G (p.Pro166=)	rs200336355
NM_001039958.2(MESP2):c.549_584del (p.180_181QG[7])	rs749710849
NM_001039958.2(MESP2):c.552GGGGCA[1] (p.180QG[11])	rs56192595

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