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rs80338842(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs80338842
GeneSDHD, TIMM8B
Chromosome11
Position112,086,910
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6.2 Hereditary PGL/PCC Syndrome
(C;G) 6.2 Hereditary PGL/PCC Syndrome
(G;G) 0 common in clinvar