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rs778376925(C;C)

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common in clinvar

Is a	genotype
of	rs778376925
Gene	STK11
Chromosome	19
Position	1,207,093
mentioned	by

0

Good

Geno	Mag	Summary
(A;C)	5.8	STK11 gene mutation associated with Peutz-Jeghers syndrome
(C;C)	0	common in clinvar
(C;G)	5.8	STK11 gene mutation associated with Peutz-Jeghers syndrome

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Is a genotype