ClinVar for MedGen (Select 75520) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2433515	NM_002332.3(LRP1):c.7896C>A (p.Asp2632Glu)	LRP1 (D2632E)	Single nucleotide variant (missense variant)	Keratosis pilaris atrophicans	GUncertain significance
Select item 2433514	NM_002332.3(LRP1):c.8999A>G (p.His3000Arg)	LRP1 (H3000R)	Single nucleotide variant (missense variant)	Keratosis pilaris atrophicans	GUncertain significance