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rs28933696(C;C)

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common in clinvar

Is a	genotype
of	rs28933696
Gene	NOTCH3
Chromosome	19
Position	15,192,134
mentioned	by

0

Good

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

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Is a genotype