Disease: Handgrip myotonia ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057518865
rs1057518865 		17 63957443 missense variant C/T snv
CUI: C1868623
Disease: Handgrip myotonia
Handgrip myotonia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.700 0
dbSNP: rs914586984
rs914586984 		1.000 0.120 17 63959275 missense variant G/C;T snv
CUI: C1868623
Disease: Handgrip myotonia
Handgrip myotonia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.700 0