List of variants in gene TNR reported as uncertain significance for Parkinson disease

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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: 5

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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_003285.3(TNR):c.1732C>T (p.Arg578Ter)	rs869312899

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