List of variants in gene GIGYF2 reported as benign for Parkinson disease 11, autosomal dominant, susceptibility to

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001103146.3(GIGYF2):c.2940A>G (p.Gln980=)	rs3816334	0.68380
NM_001103146.3(GIGYF2):c.3684+15G>A	rs6437074	0.68355
NM_001103146.3(GIGYF2):c.3461-9G>A	rs2305137	0.65200
NM_001103146.3(GIGYF2):c.3630_3632del (p.Gln1216del)	rs10555297	0.61215
NM_001103146.3(GIGYF2):c.3651G>A (p.Pro1217=)	rs12328151	0.16603
NM_001103146.3(GIGYF2):c.1554G>A (p.Glu518=)	rs2305138	0.07935
NM_001103146.3(GIGYF2):c.3629_3630insGC (p.Gln1211fs)	rs371622656

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