Related gene-specific medical variations for Gene (Select 9796) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2309413	NM_014759.5(PHYHIP):c.135G>C (p.Glu45Asp)	LOC126860324, PHYHIP (E45D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260625	NM_014759.5(PHYHIP):c.39C>A (p.Asn13Lys)	LOC126860324, PHYHIP (N13K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance