"GPD2-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3048119	NM_000408.5(GPD2):c.135C>T (p.Cys45=)	GPD2	Single nucleotide variant (synonymous variant)	GPD2-related disorder	GLikely benign
Select item 3048014	NM_000408.5(GPD2):c.579T>C (p.Tyr193=)	GPD2	Single nucleotide variant (synonymous variant)	GPD2-related disorder	GLikely benign
Select item 3048678	NM_000408.5(GPD2):c.580G>A (p.Val194Ile)	GPD2 (V194I)	Single nucleotide variant (missense variant)	GPD2-related disorder	GBenign
Select item 713776	NM_000408.5(GPD2):c.922A>G (p.Ile308Val)	GPD2 (I308V)	Single nucleotide variant (missense variant)	GPD2-related disorder +1 more	GBenign/Likely benign
Select item 3041504	NM_000408.5(GPD2):c.1224C>G (p.Pro408=)	GPD2	Single nucleotide variant (synonymous variant)	GPD2-related disorder	GLikely benign
Select item 3037525	NM_000408.5(GPD2):c.1726C>G (p.Leu576Val)	GPD2 (L576V)	Single nucleotide variant (missense variant)	GPD2-related disorder	GLikely benign

ClinVar