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rs104894306(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs104894306
GeneSDHD, TIMM8B
Chromosome11
Position112,087,868
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6.2 Hereditary PGL/PCC Syndrome

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