Related gene-specific medical variations for Gene (Select 79056) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3310600	NM_024081.6(PRRG4):c.16G>A (p.Val6Ile)	CCDC73, LOC130005485 +1 more (V6I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3310599	NM_024081.6(PRRG4):c.61T>G (p.Cys21Gly)	LOC130005486, PRRG4 (C21G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610967	NM_024081.6(PRRG4):c.85A>G (p.Lys29Glu)	LOC130005486, PRRG4 (K29E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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