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rs5030737(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs5030737
GeneMBL2
Chromosome10
Position52,771,482
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 1.1 carrier of mannose binding deficiency but of low clinical importance
(T;T) 1.6 mannose binding deficiency but of low clinical importance