rs1554436510, CLCN1

N. diseases: 2
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.
EMG: myotonic discharges
CUI: C4022169
Disease: EMG: myotonic discharges
3 7 143331279 missense variant T/C snv 0.700 0
Myotonia
CUI: C0027125
Disease: Myotonia
7 7 143331279 missense variant T/C snv 0.700 0