rs76871093(C;C)

common in clinvar

Is a	genotype
of	rs76871093
Gene	SMN1
Chromosome	5
Position	70,946,163
Merged from	Rs104893925
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	carrier of a spinal muscular atrophy disease allele
(T;T)	6	Spinal muscular atrophy, type 2 or 3