rs797044999, LGI1

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.
Epilepsy, Familial Temporal Lobe 1
CUI: C4551957
Disease: Epilepsy, Familial Temporal Lobe 1
17 0.925 0.120 10 93797547 missense variant C/T snv 0.700 1.000 1 2004 2004
Autosomal Dominant Lateral Temporal Lobe Epilepsy
CUI: C1838062
Disease: Autosomal Dominant Lateral Temporal Lobe Epilepsy
4 0.925 0.120 10 93797547 missense variant C/T snv 0.020 1.000 2 2017 2019