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rs76871093(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs76871093
GeneSMN1
Chromosome5
Position70,241,990
Merged fromRs104893925
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 carrier of a spinal muscular atrophy disease allele
(T;T) 6 Spinal muscular atrophy, type 2 or 3