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: rs137853325
rs137853325
IKBKG
2 0.925 0.160 X 154564450 missense variant T/C snv 0.700 1.000 9 2000 2011
dbSNP: rs137853326
rs137853326
IKBKG
3 0.882 0.160 X 154564451 missense variant G/A;T snv 0.700 1.000 9 2000 2011
dbSNP: rs137853327
rs137853327
IKBKG
3 0.882 0.160 X 154564418 missense variant A/T snv 0.700 1.000 9 2000 2011
dbSNP: rs137853328
rs137853328
IKBKG
2 0.925 0.160 X 154558590 missense variant T/G snv 0.700 1.000 9 2000 2011
dbSNP: rs137853330
rs137853330
IKBKG
2 0.925 0.160 X 154562904 missense variant C/G snv 0.700 1.000 9 2000 2011
dbSNP: rs179363867
rs179363867
IKBKG
2 0.925 0.160 X 154563577 missense variant G/A snv 0.700 1.000 9 2000 2011
dbSNP: rs179363868
rs179363868
IKBKG
1 1.000 0.160 X 154560412 missense variant G/C snv 0.700 1.000 9 2000 2011
dbSNP: rs179363869
rs179363869
IKBKG
1 1.000 0.160 X 154561696 missense variant T/C snv 0.700 1.000 9 2000 2011