ClinVar Miner

List of variants in gene VPS13C 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: 2
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HGVS dbSNP
NM_020821.3(VPS13C):c.387C>T (p.Gly129=) rs139665824
NM_020821.3(VPS13C):c.9020G>A (p.Arg3007Gln) rs778287890

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