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rs63750737(AA;AA)

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common in clinvar

Is a	genotype
of	rs63750737
Gene	MSH2
Chromosome	2
Position	47,470,999
mentioned	by

0

Good

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

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Is a genotype