Related gene-specific medical variations for Gene (Select 8886) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3080904	NM_006773.4(DDX18):c.56A>G (p.Lys19Arg)	DDX18, LOC112806040 (K19R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610393	NM_006773.4(DDX18):c.14C>T (p.Pro5Leu)	DDX18, LOC112806040 (P5L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274778	NM_006773.4(DDX18):c.83A>G (p.Gln28Arg)	DDX18, LOC112806040 (Q28R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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