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rs527853872(T;T)

From SNPedia

common in clinvar
Is agenotype
ofrs527853872
GeneSLC52A3
Chromosome20
Position765,372
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 8 Brown-Vialetto-Van Laere syndrome type 1 mutation; riboflavin treatment recommended
(C;T) 3 Carrier of a Brown-Vialetto-Van Laere syndrome mutation
(T;T) 0 common in clinvar