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rs587779413(C;C)

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common in clinvar

Is a	genotype
of	rs587779413
Gene	TCIRG1
Chromosome	11
Position	68,050,224
mentioned	by

0

Good

Geno	Mag	Summary
(A;C)	8.2	Severe congenital neutropenia, type 1, autosomal dominant
(C;C)	0	common in clinvar

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Is a genotype