Related gene-specific medical variations for Gene (Select 284348) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3121693	NM_001031749.3(LYPD5):c.238G>C (p.Gly80Arg)	LOC130064620, LYPD5 (G80R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121692	NM_001031749.3(LYPD5):c.199C>A (p.Arg67Ser)	LOC130064620, LYPD5 (R24S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance