rs80356687, CLCN1

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Generalized Myotonia of Thomsen
CUI: C2936781
Disease: Generalized Myotonia of Thomsen
61 0.882 0.120 7 143324442 missense variant C/T snv 1.2E-05 2.1E-05 0.710 1.000 1 2002 2002
Myotonia Congenita
CUI: C0027127
Disease: Myotonia Congenita
38 0.882 0.120 7 143324442 missense variant C/T snv 1.2E-05 2.1E-05 0.710 1.000 1 2002 2002
Becker Generalized Myotonia
CUI: C0751360
Disease: Becker Generalized Myotonia
67 0.882 0.120 7 143324442 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0