ClinVar Miner

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

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_003285.2(TNR):c.1732C>T (p.Arg578Ter) rs869312899
NM_003285.2(TNR):c.1774A>G (p.Thr592Ala) rs140481433
NM_003285.2(TNR):c.463T>A (p.Cys155Ser) rs150331590
NM_003285.2(TNR):c.496A>G (p.Thr166Ala) rs147204644
NM_003285.2(TNR):c.538A>C (p.Asn180His) rs61731112

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