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rs267608087(A;A)

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common in clinvar

Is a	genotype
of	rs267608087
Gene	MSH6
Chromosome	2
Position	47,803,508
Merged from	Rs748452299
mentioned	by

0

Good

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

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Is a genotype