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rs387906461(G;G)

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common in clinvar

Is a	genotype
of	rs387906461
Gene	F8
Chromosome	X
Position	154,902,117
mentioned	by

0

Good

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

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Is a genotype