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rs80356690(C;G)

From SNPedia

Myotonia congenita; Thomsen's disease; quite variable in degree
Is agenotype
ofrs80356690
GeneCLCN1
Chromosome7
Position143,330,788
Merged fromRs121912804
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 4 Myotonia congenita; Thomsen's disease; quite variable in degree

See discussion at myotonia congenita