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rs2272783(C;T)

From SNPedia

Low expression variant of FECH enzyme
Is agenotype
ofrs2272783
GeneFECH
Chromosome18
Position57,571,588
mentionedby
Magnitude2.2
ReputeBad
Geno Mag Summary
(C;C) 4 likely erythropoietic protoporphyria symptoms
(C;T) 2.2 Low expression variant of FECH enzyme
(T;T) 0 common in clinvar

If your other FECH allele is normal, you are most likely asymptomatic. However, if you harbor this rs2272783(C;T) genotype AND your other FECH allele is actually nonfunctional, you are likely to have symptoms associated with Erythropoietic protoporphyria.