C1864997[trait identifier] AND "Center for Genomics, Ann and Robert H. - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 234588	NM_001375808.2(LPIN2):c.2625G>A (p.Pro875=)	LPIN2	Single nucleotide variant (synonymous variant)	LPIN2-related condition +3 more	GConflicting classifications of pathogenicity
Select item 626132	NM_001375808.2(LPIN2):c.2445T>C (p.Asp815=)	LPIN2	Single nucleotide variant (synonymous variant)	LPIN2-related condition +3 more	GConflicting classifications of pathogenicity
Select item 97814	NM_001375808.2(LPIN2):c.1510C>T (p.Leu504Phe)	LPIN2 (L504F)	Single nucleotide variant (missense variant)	LPIN2-related condition +4 more	GConflicting classifications of pathogenicity
Select item 663796	NM_001375808.2(LPIN2):c.1367C>T (p.Thr456Ile)	LPIN2 (T456I)	Single nucleotide variant (missense variant)	Majeed syndrome +1 more	GUncertain significance
Select item 21520	NM_001375808.2(LPIN2):c.991G>T (p.Ala331Ser)	LPIN2 (A331S)	Single nucleotide variant (missense variant)	Autoinflammatory syndrome +3 more	GConflicting classifications of pathogenicity
Select item 234843	NM_001375808.2(LPIN2):c.959C>T (p.Thr320Ile)	LPIN2 (T320I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 579910	NM_001375808.2(LPIN2):c.584C>T (p.Ala195Val)	LPIN2 (A195V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar