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rs63749932(C;C)

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common in clinvar

Is a	genotype
of	rs63749932
Gene	MSH2
Chromosome	2
Position	47,476,399
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Lynch syndrome; pathogenic mutation
(T;T)	6	Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)

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Is a genotype