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rs886037611(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs886037611
GeneFXN
Chromosome9
Position69,035,939
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 6 Friedreich's ataxia
(-;C) 3 Carrier of a Friedreich's ataxia mutation
(C;C) 0 common in clinvar