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rs80356699(A;G)

From SNPedia

Myotonia congenita; Thomsen's disease; quite variable in degree
Is agenotype
ofrs80356699
GeneCLCN1
Chromosome7
Position143,320,744
Merged fromRs121912809
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 4 Myotonia congenita; Thomsen's disease; quite variable in degree

See discussion at myotonia congenita