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rs387906451(C;C)

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common in clinvar

Is a	genotype
of	rs387906451
Gene	F8
Chromosome	X
Position	154,930,098
mentioned	by

0

Good

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

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Is a genotype