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rs104894307(A;A)

From SNPedia
common in complete genomics
Is agenotype
ofrs104894307
GeneSDHD, TIMM8B
Chromosome11
Position112,086,908
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in complete genomics
(A;G) 6.2 Hereditary PGL/PCC Syndrome
(A;T) 6.2 Hereditary PGL/PCC Syndrome

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