Source: BEFREE ×
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: rs1057519825
rs1057519825
BTK
6 0.882 0.120 X 101356176 missense variant C/G snv 0.010 1.000 1 2014 2014
dbSNP: rs1057519826
rs1057519826
BTK
6 0.882 0.120 X 101356177 missense variant A/T snv 0.010 1.000 1 2014 2014
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2010 2010
dbSNP: rs1800890
rs1800890
IL19
29 0.658 0.400 1 206776020 intron variant A/T snv 0.32 0.010 1.000 1 2010 2010
dbSNP: rs2509049
rs2509049
H2AX
6 0.827 0.160 11 119095811 upstream gene variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs604714
rs604714
DPAGT1
3 0.925 0.120 11 119099986 intron variant C/A snv 0.31 0.010 1.000 1 2013 2013