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rs104893932(A;A)

From SNPedia

common in clinvar
Is agenotype
ofrs104893932
GeneSMN1
Chromosome5
Position70,241,953
mentionedby
Magnitude0
ReputeGood
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