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rs121908936(A;T)

From SNPedia

Carrier of a congenital lactase deficiency allele
Is agenotype
ofrs121908936
GeneLCT
Chromosome2
Position135,807,131
mentionedby
Magnitude2.5
ReputeBad
Geno Mag Summary
(A;A) 5 Congenital lactase deficiency
(A;T) 2.5 Carrier of a congenital lactase deficiency allele
(T;T) 0 common in clinvar

In the absence of other mutations in this gene (LCT), this genotype represents an unaffected carrier. In the presence of another LCT mutation, though, this genotype could be associated with congenital lactase deficiency.