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: rs764343290
rs764343290
FOXG1
1 1.000 0.120 14 28768302 stop gained C/G;T snv 4.0E-06 0.700 1.000 2 2010 2010
dbSNP: rs121913678
rs121913678
FOXG1
1 1.000 0.120 14 28768044 stop gained G/A;T snv 0.700 0
dbSNP: rs138747073
rs138747073
FOXG1
2 0.925 0.120 14 28768479 stop gained C/A;G;T snv 6.0E-05 0.700 0
dbSNP: rs1555321237
rs1555321237
FOXG1
1 1.000 0.120 14 28767493 stop gained C/T snv 0.700 0
dbSNP: rs1555321351
rs1555321351
FOXG1
1 1.000 0.120 14 28768043 stop gained G/A snv 0.700 0
dbSNP: rs267606826
rs267606826
FOXG1
38 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
dbSNP: rs267606827
rs267606827
FOXG1
3 0.925 0.120 14 28768203 stop gained G/A snv 0.700 0
dbSNP: rs398124202
rs398124202
FOXG1
1 1.000 0.120 14 28767535 stop gained C/A;G;T snv 0.700 0
dbSNP: rs587783642
rs587783642
FOXG1
1 1.000 0.120 14 28768041 stop gained C/G snv 0.700 0
dbSNP: rs786204999
rs786204999
FOXG1
1 1.000 0.120 14 28768527 stop gained C/G;T snv 8.0E-06 0.700 0
dbSNP: rs267606828
rs267606828
FOXG1
1 1.000 0.120 14 28767922 missense variant T/C snv 0.800 1.000 3 2010 2016
dbSNP: rs786205009
rs786205009
FOXG1
1 1.000 0.120 14 28768009 missense variant C/T snv 0.800 1.000 3 2011 2014
dbSNP: rs767961672
rs767961672
FOXG1
4 0.925 0.200 14 28767822 missense variant G/A;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs1057516138
rs1057516138
FOXG1
1 1.000 0.120 14 28767833 missense variant G/C;T snv 0.700 0
dbSNP: rs1064797186
rs1064797186
FOXG1
1 1.000 0.120 14 28767964 missense variant A/C snv 0.700 0
dbSNP: rs1555321337
rs1555321337
FOXG1
1 1.000 0.120 14 28767992 missense variant G/A snv 0.700 0
dbSNP: rs1555321361
rs1555321361
FOXG1
1 1.000 0.120 14 28768103 missense variant G/C snv 0.700 0
dbSNP: rs1566445489
rs1566445489
FOXG1
1 1.000 0.120 14 28767982 missense variant C/T snv 0.700 0
dbSNP: rs1566445533
rs1566445533
FOXG1
1 1.000 0.120 14 28768042 missense variant T/A snv 0.700 0
dbSNP: rs587783640
rs587783640
FOXG1
1 1.000 0.120 14 28768034 missense variant G/T snv 0.700 0
dbSNP: rs587783641
rs587783641
FOXG1
1 1.000 0.120 14 28768036 missense variant A/G snv 0.700 0
dbSNP: rs587783643
rs587783643
FOXG1
1 1.000 0.120 14 28768078 missense variant G/A snv 0.700 0
dbSNP: rs727503935
rs727503935
FOXG1
1 1.000 0.120 14 28767949 missense variant G/A snv 0.700 0
dbSNP: rs786204998
rs786204998
FOXG1
1 1.000 0.120 14 28767923 missense variant TC/CT mnv 0.700 0
dbSNP: rs786205005
rs786205005
FOXG1
1 1.000 0.120 14 28767856 missense variant G/A snv 0.700 0