rs104893932(A;A)

common in clinvar

Is a	genotype
of	rs104893932
Gene	SMN1
Chromosome	5
Position	70,946,126
mentioned	by

Magnitude

0

Repute

Good

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