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rs11214077(A;G)

From SNPedia
classified as benign variant in ClinVar
Is agenotype
ofrs11214077
GeneSDHD, TIMM8B
Chromosome11
Position112,087,953
mentionedby
Magnitude1
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)

see rs11214077