rs113993961(C;C)

Werner syndrome; homozygote for transversion mutation

Is a	genotype
of	rs113993961
Gene	WRN
Chromosome	8
Position	31,141,680
mentioned	by

Magnitude

6

Repute

Bad

Geno	Mag	Summary
(C;C)	6	Werner syndrome; homozygote for transversion mutation
(C;G)	2	carrier for Werner syndrome
(G;G)	0	normal