Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs797044999
rs797044999
LGI1
2 0.925 0.120 10 93797547 missense variant C/T snv 0.020 1.000 2 2017 2019
dbSNP: rs104894166
rs104894166
LGI1 ; LOC101927013
3 0.882 0.120 10 93758280 missense variant T/C snv 0.010 1.000 1 2002 2002
dbSNP: rs1064794249
rs1064794249
LGI1
2 0.925 0.120 10 93797550 missense variant G/A snv 0.010 1.000 1 2019 2019
dbSNP: rs778672052
rs778672052
ADAM22 ; LOC105375386
2 0.925 0.120 7 88149056 missense variant A/G snv 8.1E-06 0.010 1.000 1 2019 2019