Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2270565
UCP1
0.882 0.080 4 140562317 missense variant T/A snv 8.9E-02 6.5E-02 4
rs7612463
UBE2E2
0.925 0.080 3 23294959 intron variant C/A;G snv 3
rs3737787
TSTD1 ; USF1
0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs12472151
TRPM8
1.000 0.040 2 233944048 intron variant G/A snv 4.2E-02 1
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs17110690
TPH2
0.925 0.080 12 72014217 intron variant G/A snv 0.19 2
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 8
rs767455
TNFRSF1A
0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 13
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5030728
TLR4
0.807 0.160 9 117712004 intron variant G/A;T snv 0.23 7
rs1003880422
TH
0.925 0.080 11 2166716 missense variant G/A;T snv 6.9E-06 2
rs3773651
TGFBR2
1.000 0.040 3 30677040 intron variant A/G snv 3.9E-02 1
rs2206277
TFAP2B
0.925 0.080 6 50830813 intron variant C/T snv 0.19 4
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs10749127
TCF7L2
1.000 0.040 10 113089594 intron variant C/T snv 0.28 1
rs565119818
TCF7L2
1.000 0.040 10 113151854 synonymous variant C/T snv 1.6E-05 1
rs575072438
TCF7L2
1.000 0.040 10 113152371 synonymous variant C/T snv 2.8E-05 2.1E-05 1
rs10850335
TBX5
0.925 0.200 12 114375303 intron variant T/C snv 3.1E-02 2
rs1981529
STEAP4
0.925 0.080 7 88284046 missense variant C/A;T snv 0.78 2