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rs137852388(A;A)

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common in clinvar

Is a	genotype
of	rs137852388
Gene	F8
Chromosome	X
Position	154,993,141
Merged from	Rs28935209
mentioned	by

0

Good

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

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Is a genotype