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rs28937321(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs28937321
GeneNOTCH3
Chromosome19
Position15,192,504
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 7.7 Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukocenphalopathy, type 1 (CADASIL)