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rs267607069(C;T)

From SNPedia
Carrier of an infantile Parkinsonism-dystonia mutation
Is agenotype
ofrs267607069
GeneSLC6A3
Chromosome5
Position1,411,328
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of an infantile Parkinsonism-dystonia mutation
(T;T) 8 Infantile Parkinsonism-dystonia

Unaffected in absence of a second SLC6A3 mutation; see SLC6A3