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rs137852272(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs137852272
GeneF9
ChromosomeX
Position139,548,455
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3.5 Carrier of a Hemophilia B mutation
(T;T) 5.5 Hemophilia B (severity varies)