Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs1017621656
TGFB1
0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05 3
rs2736118
TERT
0.882 0.120 5 1260080 intron variant T/C snv 0.33 4
rs4135113
TDG
0.925 0.080 12 103982915 missense variant G/A;C;T snv 4.7E-02 5
rs1425164489
TCN2
0.925 0.080 22 30617374 missense variant A/G;T snv 4.0E-06 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 11
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs121913314
SRC
0.851 0.120 20 37403359 stop gained C/T snv 5
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs4464148
SMAD7
0.827 0.120 18 48932662 intron variant T/C snv 0.25 7
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs764986276
SHMT1
0.925 0.080 17 18333172 missense variant C/G;T snv 4.0E-06; 4.4E-05 2
rs757128066
RIN1
0.925 0.080 11 66334745 missense variant C/A;T snv 6.9E-06; 5.5E-05 2
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 13
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15
rs11923427
RAF1
0.925 0.080 3 12622336 intron variant C/G;T snv 2