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rs80356696(A;A)

From SNPedia

common in clinvar
Is agenotype
ofrs80356696
GeneCLCN1
Chromosome7
Position143,342,001
Merged fromRs121912803
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 4 Myotonia congenita; Thomsen's disease; quite variable in degree