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rs28933698(T;T)

From SNPedia
common in clinvar
Is agenotype
ofrs28933698
GeneNOTCH3
Chromosome19
Position15,189,004
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;T) 7.7 Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukocenphalopathy, type 1 (CADASIL)
(T;T) 0 common in clinvar