List of variants reported as uncertain significance for Parkinson disease 11, autosomal dominant, susceptibility to

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001103146.3(GIGYF2):c.73A>G (p.Thr25Ala)	rs115263050	0.00024
NM_001103146.3(GIGYF2):c.2378C>T (p.Ala793Val)	rs748538823	0.00006
NM_001103146.3(GIGYF2):c.1615A>C (p.Lys539Gln)
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.3630_3635del (p.Gln1215_Gln1216del)
NM_001103146.3(GIGYF2):c.41+4A>G
NM_001103146.3(GIGYF2):c.851G>C (p.Ser284Thr)

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