Have questions? Visit https://www.reddit.com/r/SNPedia

rs397514661(C;T)

From SNPedia

Jump to:navigation, search

Carrier of an infancy diarrhea mutation

Is a	genotype
of	rs397514661
Gene	EPCAM
Chromosome	2
Position	47,374,035
mentioned	by

3

Bad

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Carrier of an infancy diarrhea mutation

Unaffected in absence of a second EPCAM gene mutation

Retrieved from "https://www.SNPedia.com/index.php?title=Rs397514661(C;T)&oldid=1691881"

Is a genotype