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: rs755500591
rs755500591
LGI4
1 1.000 19 35126873 missense variant C/G;T snv 8.1E-06; 4.0E-06 0.800 1.000 1 2017 2017
dbSNP: rs1064797094
rs1064797094
LGI4
1 1.000 19 35125506 missense variant A/T snv 7.0E-06 0.800 0
dbSNP: rs1064797093
rs1064797093
LGI4
1 1.000 19 35126848 missense variant C/G snv 0.700 0
dbSNP: rs1064797095
rs1064797095
LGI4
1 1.000 19 35126265 missense variant C/A;T snv 4.1E-06 0.700 0
dbSNP: rs1366269616
rs1366269616
LGI4
1 1.000 19 35126416 stop gained G/A snv 1.4E-05 0.700 0
dbSNP: rs1555734932
rs1555734932
LGI4
1 1.000 19 35134075 missense variant A/C snv 0.700 0
dbSNP: rs775997446
rs775997446
LGI4
1 1.000 19 35126706 stop gained C/A;G;T snv 7.5E-06; 2.2E-05 0.700 0
dbSNP: rs779232987
rs779232987
LGI4
1 1.000 19 35126853 missense variant C/T snv 2.5E-05 1.4E-05 0.700 0