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rs118192171(AC;TT)

From SNPedia

likely severe central core disease
Is agenotype
ofrs118192171
GeneRYR1
Chromosome19
Position38,585,057
mentionedby
Magnitude5
ReputeBad
Geno Mag Summary
(AC;TT) 5 likely severe central core disease
(TT;TT) 0 common in clinvar

Apparently leads to a dominant form of this myopathy.