rs104893935(C;C)

common in clinvar

Is a	genotype
of	rs104893935
Gene	SMN1
Chromosome	5
Position	70,942,416
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	3	carrier of a spinal muscular atrophy disease allele
(G;G)	6	Spinal muscular atrophy, type 1 or 2