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rs71799110(C;G)

From SNPedia
Carrier of a Parkinson disease mutation
Is agenotype
ofrs71799110
GeneFBXO7
Chromosome22
Position32,493,269
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 Carrier of a Parkinson disease mutation
(G;G) 7 Parkinson disease, type 15

Unaffected in absence of a second mutation in the FBXO7 gene