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rs764313717(C;T)

From SNPedia
Carrier of a McArdle disease mutation (mild form)
Is agenotype
ofrs764313717
GenePYGM
Chromosome11
Position64,758,375
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 5 McArdle disease, mild form (also known as glycogen storage disease type V)
(T;T) 0 common in clinvar

Unaffected in absence of a second mutation in the PYGM gene