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rs41309766(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs41309766
GeneNOTCH1
Chromosome9
Position136,505,384
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;C) 4 Possibly pathogenic for an aortic valve disorder
(C;C) 0 common in clinvar