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rs28933696(G;G)

From SNPedia
Is agenotype
ofrs28933696
GeneNOTCH3
Chromosome19
Position15,192,134
mentionedby
Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 7.7 Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukocenphalopathy, type 1 (CADASIL)
(G;G) 0