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rs878854594(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs878854594
GeneSDHD
Chromosome11
Position112,094,851
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6.2 Hereditary PGL/PCC Syndrome

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