List of variants in gene FAT4 reported as benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001291303.3(FAT4):c.2944T>C (p.Leu982=)	rs2940779	0.74871
NM_001291303.3(FAT4):c.14604A>G (p.Arg4868=)	rs1014866	0.74715
NM_001291303.3(FAT4):c.4305C>T (p.Ile1435=)	rs2710555	0.73896
NM_001291303.3(FAT4):c.2420C>T (p.Ala807Val)	rs1039808	0.46652
NM_001291303.3(FAT4):c.10577G>A (p.Gly3526Asp)	rs1567047	0.21721
NM_001291303.3(FAT4):c.405C>T (p.Phe135=)	rs72928772	0.17506
NM_001291303.3(FAT4):c.1358A>T (p.Gln453Leu)	rs6847454

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