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rs63750439(TA;TA)

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common in clinvar

Is a	genotype
of	rs63750439
Gene	MSH6
Chromosome	2
Position	47,799,173
mentioned	by

0

Good

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

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Is a genotype