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rs71799110(C;C)

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common in clinvar

Is a	genotype
of	rs71799110
Gene	FBXO7
Chromosome	22
Position	32,493,269
mentioned	by

0

Good

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

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Is a genotype