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rs137852269(T;T)

From SNPedia
common in clinvar
Is agenotype
ofrs137852269
GeneF9
ChromosomeX
Position139,562,042
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 5.5 Hemophilia B (severity varies)
(C;T) 3.5 Carrier of a Hemophilia B mutation
(T;T) 0 common in clinvar