rs2266886(C;T)

0.26x reduced risk for Meniere's disease

Is a	genotype
of	rs2266886
Gene	HCFC1
Chromosome	X
Position	153,965,901
mentioned	by

Geno	Mag	Summary
(C;C)		normal
(C;T)		0.26x reduced risk for Meniere's disease
(T;T)		0.26x reduced risk for Meniere's disease