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rs267606993(A;A)

From SNPedia

common in clinvar
Is agenotype
ofrs267606993
GenePYGM
Chromosome11
Position64,759,898
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) Carrier of a McArdle disease mutation
(C;C) 5 McArdle disease (also known as glycogen storage disease type V)