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rs137852238(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs137852238
GeneF9
ChromosomeX
Position139,551,113
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 5.5 Hemophilia B (severity varies)
(A;G) 3.5 Carrier of a Hemophilia B mutation
(G;G) 0 common in clinvar