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rs104894108(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs104894108
GeneFXN
Chromosome9
Position69,035,785
Merged fromRs28942069
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 6 Friedreich's ataxia
(A;G) 3 carrier of a Friedreich's ataxia allele
(G;G) 0 common in clinvar
(G;T) 3 carrier of a Friedreich's ataxia allele
(T;T) 6 Friedreich's ataxia