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rs587776647(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs587776647
GeneSDHD
Chromosome11
Position112,094,953
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;A) 6.2 Hereditary PGL/PCC Syndrome
(A;A) 0 common in clinvar

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