List of variants reported as uncertain significance for Parkinson disease

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_003285.3(TNR):c.496A>G (p.Thr166Ala)	rs147204644	0.00407
NM_003285.3(TNR):c.538A>C (p.Asn180His)	rs61731112	0.00326
NM_003285.3(TNR):c.1774A>G (p.Thr592Ala)	rs140481433	0.00028
NM_003285.3(TNR):c.463T>A (p.Cys155Ser)	rs150331590	0.00006
NM_001382273.1(TNK2):c.1088T>C (p.Val363Ala)	rs370013968	0.00005
NM_001382273.1(TNK2):c.2981C>T (p.Ala994Val)	rs571171423	0.00004
NM_001382273.1(TNK2):c.1957G>A (p.Val653Met)	rs201407161
NM_003285.3(TNR):c.1732C>T (p.Arg578Ter)	rs869312899
NM_198578.4(LRRK2):c.1147A>C (p.Ser383Arg)
NM_198578.4(LRRK2):c.4310A>G (p.Asn1437Ser)	rs1944946235

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