Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs121908119
WNT10A ; LOC107984111
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10
rs121909636
FGFR1
0.827 0.240 8 38414569 stop gained G/A snv 7
rs121909635
FGFR1
0.827 0.240 8 38426158 missense variant C/T snv 6
rs267606805
FGFR1
0.851 0.240 8 38414173 missense variant G/T snv 5
rs267606806
FGFR1
0.851 0.240 8 38414166 missense variant G/A;C snv 1.2E-05 5
rs3811046
IL37
0.851 0.160 2 112913801 missense variant G/A;T snv 4.0E-06; 0.71 5