List of variants in gene FHL2 reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001318895.3(FHL2):c.156+2T>C	rs727503059	0.00001
NM_001318895.3(FHL2):c.62T>A (p.Leu21Gln)	rs755805016
NM_001318895.3(FHL2):c.81C>A (p.Tyr27Ter)	rs727503060

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