C4083045[trait identifier] AND "Clinical Genetics DNA and cytogenetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 522283	NM_001103146.3(GIGYF2):c.1554G>A (p.Glu518=)	GIGYF2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 518336	NM_001103146.3(GIGYF2):c.2940A>G (p.Gln980=)	GIGYF2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 518337	NM_001103146.3(GIGYF2):c.3461-9G>A	GIGYF2	Single nucleotide variant (intron variant)	Parkinson disease 11, autosomal dominant, susceptibility to +1 more	GBenign
Select item 402899	NM_001103146.3(GIGYF2):c.3629_3630insGC (p.Gln1211fs)	GIGYF2 (Q1211fs +2 more)	Insertion (frameshift variant +1 more)	not specified +2 more	GBenign/Likely benign
Select item 518339	NM_001103146.3(GIGYF2):c.3651G>A (p.Pro1217=)	GIGYF2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 518340	NM_001103146.3(GIGYF2):c.3684+15G>A	GIGYF2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar