Related gene-specific medical variations for Gene (Select 5125) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3305254	NM_001372043.1(PCSK5):c.446A>G (p.Asp149Gly)	LOC126860646, PCSK5 (D149G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614281	NM_001372043.1(PCSK5):c.488A>G (p.Lys163Arg)	LOC126860646, PCSK5 (K163R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595850	NM_001372043.1(PCSK5):c.439C>G (p.Gln147Glu)	LOC126860646, PCSK5 (Q147E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384149	NM_001372043.1(PCSK5):c.425A>G (p.Asn142Ser)	LOC126860646, PCSK5 (N142S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 786572	NM_001372043.1(PCSK5):c.447C>T (p.Asp149=)	LOC126860646, PCSK5	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 218535	NM_001372043.1(PCSK5):c.555C>T (p.Tyr185=)	LOC126860646, PCSK5	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GUncertain significance

ClinVar