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rs63749821(-;-)

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common in clinvar

Is a	genotype
of	rs63749821
Gene	MSH6
Chromosome	2
Position	47,803,446
mentioned	by

0

Good

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;TA)	6	Likely miscall in Ancestry data; otherwise, Lynch syndrome, pathogenic mutation
(I;I)	0

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Is a genotype