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rs10513789(T;T)

From SNPedia

Very common. Normal risk of Parkinson's disease.
Is agenotype
ofrs10513789
GeneMCCC1
Chromosome3
Position183,042,285
mentionedby
Magnitude1.25
Geno Mag Summary
(G;G) 1.5 lower risk of Parkinson's disease
(G;T) 2 increased risk of Parkinson's disease
(T;T) 1.25 Very common. Normal risk of Parkinson's disease.

Approximately 55% of non-asian people have this genotype which is associated with slightly higher risk of Parkinson's disease when compared to genotype (G;G).

It is notable because it is the first SNP patented by 23andMe

rs10513789(T) increased risk of developing Parkinson's Disease

GenomicsLawReport