Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs104893932(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs104893932
GeneSMN1
Chromosome5
Position70,946,126
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