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rs137852468(G;G)

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common in clinvar

Is a	genotype
of	rs137852468
Gene	F8
Chromosome	X
Position	154,861,810
Merged from	Rs28937305
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	5.5	Hemophilia A (severity varies)
(C;G)	3.5	Carrier of a Hemophilia A mutation
(G;G)	0	common in clinvar

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Is a genotype