ClinVar Miner

List of variants reported as pathogenic for Parkinson disease 22, autosomal dominant by OMIM

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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NM_016139.4(CHCHD2):c.182C>T (p.Thr61Ile) rs864309650
NM_016139.4(CHCHD2):c.300+5G>A rs750014782
NM_016139.4(CHCHD2):c.434G>A (p.Arg145Gln) rs752169833

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