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rs33996892(A;A)

From SNPedia
common in complete genomics
Is agenotype
ofrs33996892
GeneHBB
Chromosome11
Position5,225,608
Merged fromRs121909829
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in complete genomics
(AG;AG) 0 common in clinvar

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