ClinVar Miner

List of variants in gene PRKN reported as likely benign 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_004562.3(PRKN):c.1071C>G (p.Gly357=) rs878854707
NM_004562.3(PRKN):c.1096C>T (p.Arg366Trp) rs56092260
NM_004562.3(PRKN):c.1310C>T (p.Pro437Leu) rs149953814
NM_004562.3(PRKN):c.522C>T (p.Leu174=) rs147121590
NM_004562.3(PRKN):c.919C>T (p.Leu307=) rs138920699

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