Related gene-specific medical variations for Gene (Select 400451) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2346505	NM_207446.3(FAM174B):c.193A>G (p.Ser65Gly)	FAM174B, LOC130057968 (S65G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2341249	NM_207446.3(FAM174B):c.202T>G (p.Ser68Ala)	FAM174B, LOC130057968 (S68A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance