List of variants in gene GIGYF2 studied for Parkinson disease 11, autosomal dominant, susceptibility to

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001103146.3(GIGYF2):c.2940A>G (p.Gln980=)	rs3816334	0.69457
NM_001103146.3(GIGYF2):c.3684+15G>A	rs6437074	0.69433
NM_001103146.3(GIGYF2):c.3461-9G>A	rs2305137	0.66032
NM_001103146.3(GIGYF2):c.3630_3632del (p.Gln1216del)	rs10555297	0.62170
NM_001103146.3(GIGYF2):c.3651G>A (p.Pro1217=)	rs12328151	0.16825
NM_001103146.3(GIGYF2):c.1554G>A (p.Glu518=)	rs2305138	0.07960
NM_001103146.3(GIGYF2):c.167A>G (p.Asn56Ser)	rs72554080	0.00033
NM_001103146.3(GIGYF2):c.1370A>C (p.Asn457Thr)	rs116074753	0.00032
NM_001103146.3(GIGYF2):c.1262A>G (p.Lys421Arg)	rs115735611	0.00016
NM_001103146.3(GIGYF2):c.832A>G (p.Ile278Val)	rs118203904	0.00006
NM_001103146.3(GIGYF2):c.2378C>T (p.Ala793Val)	rs748538823	0.00005
NM_001103146.3(GIGYF2):c.1818C>G (p.Asp606Glu)	rs118203903
NM_001103146.3(GIGYF2):c.2146A>G (p.Thr716Ala)	rs1700885234
NM_001103146.3(GIGYF2):c.2489A>T (p.Glu830Val)	rs1327472255
NM_001103146.3(GIGYF2):c.3629_3630insGC (p.Gln1211fs)	rs371622656

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