Related gene-specific medical variations for Gene (Select 84893) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3093271	NM_178150.3(FBH1):c.3124G>A (p.Val1042Ile)	FBH1, LOC105376384 (V1042I +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3093270	NM_178150.3(FBH1):c.3085A>T (p.Asn1029Tyr)	FBH1, LOC105376384 (N955Y +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3093269	NM_178150.3(FBH1):c.3062G>A (p.Arg1021His)	FBH1, LOC105376384 (R947H +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3093268	NM_178150.3(FBH1):c.3061C>T (p.Arg1021Cys)	FBH1, LOC105376384 (R947C +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3093251	NM_178150.3(FBH1):c.1811G>A (p.Arg604His)	FBH1, LOC126860848 (R604H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618353	NM_178150.3(FBH1):c.3076A>C (p.Thr1026Pro)	FBH1, LOC105376384 (T952P +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2608274	NM_178150.3(FBH1):c.3008C>T (p.Ala1003Val)	FBH1, LOC105376384 (A1003V +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 161784	NM_178150.3(FBH1):c.2107C>T (p.Arg703Trp)	FBH1 (R754W +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance