Related gene-specific medical variations for Gene (Select 22889) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3113996	NM_014949.4(KHDC4):c.7G>A (p.Ala3Thr)	KHDC4, LOC126805876 (A3T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525185	NM_014949.4(KHDC4):c.37G>C (p.Gly13Arg)	KHDC4, LOC126805876 (G13R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1227203	NM_014949.4(KHDC4):c.-13A>G	KHDC4, LOC126805876	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign

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