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rs63750233(C;C)

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common in clinvar

Is a	genotype
of	rs63750233
Gene	MSH2
Chromosome	2
Position	47,478,408
mentioned	by

0

Good

Geno	Mag	Summary
(-;C)	6	Lynch syndrome, pathogenic mutation
(C;C)	0	common in clinvar
(I;I)	0

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Is a genotype