Related gene-specific medical variations for Gene (Select 105377108) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2405525	NM_138805.3(FAM3D):c.588C>G (p.Phe196Leu)	FAM3D-AS1, FAM3D (F196L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2375800	NM_138805.3(FAM3D):c.598A>G (p.Ser200Gly)	FAM3D, FAM3D-AS1 (S200G)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance