List of variants in gene FGD4 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001370298.3(FGD4):c.*2487C>A	rs188600194	0.00491
NM_001370298.3(FGD4):c.167-61923G>A	rs184708096	0.00190
NM_001370298.3(FGD4):c.*4772dup	rs567814235
NM_001370298.3(FGD4):c.785C>G (p.Thr262Arg)	rs200732890

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