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rs104893927(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs104893927
GeneSMN1
Chromosome5
Position70,942,367
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;G) 3 carrier of a spinal muscular atrophy disease allele
(G;G) 0 common in clinvar