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rs876660073(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs876660073
GeneMAX
Chromosome14
Position65,076,639
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 6.2 Hereditary PGL/PCC Syndrome
(C;C) 0 common in clinvar

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