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rs139616452(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs139616452
GeneFXN
Chromosome9
Position69,072,673
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 carrier of a Friedreich's ataxia allele
(T;T) 6 Friedreich's ataxia