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rs104894308(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs104894308
GeneSDHD, TIMM8B
Chromosome11
Position112,087,933
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6.2 Hereditary PGL/PCC Syndrome
(G;G) 0 common in clinvar