rs4988235 – SNPedia

November 11, 2018

Also known as "C/T(-13910)", and located in the MCM6 gene but with influence on the lactase LCT gene, rs4988235 is one of two SNPs that is associated with the primary haplotype associated with hypolactasia, more commonly known as lactose intolerance in European Caucasian populations.

(C;C) 2.5 likely to be lactose intolerant as an adult
(C;T) 1.1 likely to be able to digest milk as an adult
(T;T) 1.1 can digest milk