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rs587776652(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs587776652
GeneSDHC
Chromosome1
Position161,314,408
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6.2 Hereditary PGL/PCC Syndrome
(G;G) 0 common in clinvar