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rs33958088(C;C)

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common in complete genomics

Is a	genotype
of	rs33958088
Gene	HBB
Chromosome	11
Position	5,226,937
Merged from	Rs121909828
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(CT;CT)	0	common in clinvar

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Is a genotype