Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs34779708
CREM
0.827 0.120 10 35177257 intron variant T/G snv 0.33 6
rs3766606
PARK7
0.827 0.120 1 7962137 intron variant G/T snv 0.22 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6
rs3853824
C17orf67
0.827 0.120 17 56803632 intron variant T/C snv 0.66 6
rs395157
OSMR
0.827 0.120 5 38867630 intron variant C/T snv 0.47 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6
rs4976646
RGS14
0.851 0.200 5 177361569 intron variant T/C snv 0.41 6
rs6062496
TNFRSF6B ; RTEL1-TNFRSF6B
0.827 0.120 20 63697746 intron variant G/A snv 0.52 6
rs6863411
NDFIP1
0.827 0.120 5 142133639 intron variant A/T snv 0.67 6
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv 6
rs7404095
PRKCB
0.827 0.120 16 23853269 intron variant T/C snv 0.58 6
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 6
rs925255
FOSL2 ; FLJ31356
0.827 0.120 2 28391927 intron variant C/T snv 0.38 6
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 6
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs12654812
RGS14
0.925 0.120 5 177367190 intron variant G/A snv 0.34 5
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 5