rs613872(T;T)

common in complete genomics

Is a	genotype
of	rs613872
Gene	TCF4
Chromosome	18
Position	55,543,071
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(G;G)	2.5	~20-30x higher risk for Fuchs' dystrophy, a corneal disorder
(G;T)	2.5	~5 fold higher risk for Fuchs' dystrophy, a corneal disorder
(T;T)	0	common in complete genomics