"Genome-Nilou Lab"[submitter] AND "PIGG"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1185383	NM_001127178.3(PIGG):c.571-563A>G	PIGG	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1170160	NM_001127178.3(PIGG):c.1743T>C (p.Leu581=)	PIGG	Single nucleotide variant (synonymous variant +1 more)	Intellectual disability, autosomal recessive 53 +1 more	GBenign
Select item 1165000	NM_001127178.3(PIGG):c.1828T>C (p.Cys610Arg)	PIGG (C244R +7 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal recessive 53 +1 more	GBenign
Select item 1165001	NM_001127178.3(PIGG):c.1989C>T (p.Ala663=)	PIGG	Single nucleotide variant (synonymous variant +1 more)	Intellectual disability, autosomal recessive 53 +1 more	GBenign
Select item 1165002	NM_001127178.3(PIGG):c.2095G>A (p.Val699Ile)	PIGG (V188I +7 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Intellectual disability, autosomal recessive 53 +1 more	GBenign
Select item 1269117	NM_001127178.3(PIGG):c.2261+49A>T	PIGG	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GBenign

ClinVar