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rs104894302(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs104894302
GeneSDHD
Chromosome11
Position112,089,002
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6.2 Hereditary PGL/PCC Syndrome