Related gene-specific medical variations for Gene (Select 55785) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2559582	NM_018351.4(FGD6):c.2384A>T (p.Glu795Val)	FGD6, LOC124646383 (E795V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2297622	NM_018351.4(FGD6):c.2390A>G (p.Tyr797Cys)	FGD6, LOC124646383 (Y797C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1340322	GRCh37/hg19 12q22(chr12:95475366-95601325)x1	FGD6	Copy number loss	not provided	GUncertain significance

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