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rs587779301(-;-)

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common in clinvar

Is a	genotype
of	rs587779301
Gene	MSH6, FBXO11
Chromosome	2
Position	47,806,650
mentioned	by

0

Good

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;ATTTC)	6	Some evidence of miscall likelihood in 23andMe v5 data; otherwise, Lynch syndrome, pathogenic mutation

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Is a genotype