Variants in gene MYH9 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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_002473.6(MYH9):c.2105G>A (p.Arg702His)	rs80338827	0.00001
NM_002473.6(MYH9):c.2114G>A (p.Arg705His)	rs80338828
NM_002473.6(MYH9):c.2152C>T (p.Arg718Trp)	rs1184544985
NM_002473.6(MYH9):c.2507C>T (p.Pro836Leu)	rs1603483077
NM_002473.6(MYH9):c.283G>A (p.Ala95Thr)	rs1603484047
NM_002473.6(MYH9):c.287C>T (p.Ser96Leu)	rs121913657
NM_002473.6(MYH9):c.5521G>A (p.Glu1841Lys)	rs80338834

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