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rs11214077(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs11214077
GeneSDHD, TIMM8B
Chromosome11
Position112,087,953
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 1 classified as benign variant in ClinVar
(G;G) 1 most likely a benign genotype according to ClinVar (although rare)