ClinVar Miner

List of variants reported as likely benign for Parkinson disease by Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_012179.4(FBXO7):c.122+9G>A rs192327462
NM_012179.4(FBXO7):c.693C>T (p.Ser231=) rs61752254
NM_022089.4(ATP13A2):c.*120A>T rs41273151
NM_022089.4(ATP13A2):c.106-8G>A rs200587951
NM_022089.4(ATP13A2):c.1195+10G>A rs55689004
NM_022089.4(ATP13A2):c.132A>G (p.Pro44=) rs200816691
NM_022089.4(ATP13A2):c.1614C>T (p.Pro538=) rs56351817
NM_022089.4(ATP13A2):c.951C>T (p.Cys317=) rs148391179

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