Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3769839
SP110 ; SP140
0.925 0.080 2 230211910 intron variant T/C snv 0.12 2
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs3219472
TOE1 ; MUTYH
0.882 0.160 1 45338378 5 prime UTR variant C/T snv 0.26 3
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs2076310
RXRB
0.925 0.080 6 33198257 intron variant A/G snv 0.27 0.28 2
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs2230054
CXCR2
0.925 0.080 2 218135587 synonymous variant C/T snv 0.48 0.54 2
rs8004738
SERPINA1
0.925 0.080 14 94390577 5 prime UTR variant G/A snv 0.55 2
rs3219476
MUTYH
0.882 0.200 1 45336998 intron variant A/C snv 0.58 3
rs1126579
CXCR2
0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62 8
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19