ClinVar Miner

List of variants reported as likely pathogenic for Parkinson disease 2

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Total variants: 5
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HGVS dbSNP
NC_000006.11:g.(?_162683537)_(162683817_?)dup
NM_001018111.3(PODXL):c.89_90insGTCGCCCC (p.Gln32fs) rs1554391082
NM_004562.3(PRKN):c.1289G>A (p.Gly430Asp) rs191486604
NM_004562.3(PRKN):c.734+1G>A rs1562430103
Single allele

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