rs7503034(T;T)

Benign (harmless) variant

Is a	genotype
of	rs7503034
Gene	SGSH
Chromosome	17
Position	80,210,594
mentioned	by

Magnitude

0.1

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	0.1	Benign (harmless) variant
(T;T)	0.1	Benign (harmless) variant