ClinVar Miner

List of variants in gene PRKN reported as likely benign for Parkinson disease

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_004562.3(PRKN):c.*1252C>T rs77926621
NM_004562.3(PRKN):c.*1407C>T
NM_004562.3(PRKN):c.*1462C>A rs11961229
NM_004562.3(PRKN):c.*15C>A rs35125035
NM_004562.3(PRKN):c.*1695G>A rs77283740
NM_004562.3(PRKN):c.*1909G>A
NM_004562.3(PRKN):c.*2187C>T
NM_004562.3(PRKN):c.*2217G>A rs138660139
NM_004562.3(PRKN):c.*2354C>T rs191130749
NM_004562.3(PRKN):c.*94A>G
NM_004562.3(PRKN):c.101A>G (p.Gln34Arg) rs148851677
NM_004562.3(PRKN):c.1071C>G (p.Gly357=) rs878854707
NM_004562.3(PRKN):c.458C>G (p.Pro153Arg) rs55654276
NM_004562.3(PRKN):c.783A>G (p.Leu261=) rs9456711
NM_004562.3(PRKN):c.814C>A (p.Leu272Ile)
NM_004562.3(PRKN):c.919C>T (p.Leu307=) rs138920699

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