Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs866294686
TRIM8 ; LOC105378460
0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs10511544
PTPRD
9 10319881 intron variant A/C snv 0.32 1
rs10756026
PTPRD
9 10337976 intron variant T/A snv 0.34 1
rs10809070
PTPRD
9 10341235 intron variant C/G snv 0.30 1
rs3741845
TAS2R9
12 10809516 missense variant A/G snv 0.60 0.51 1
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 14
rs1800038
ADRA2A
10 111079134 synonymous variant C/A snv 7.4E-02 4.9E-02 1
rs3750625
ADRA2A
10 111079843 3 prime UTR variant C/A snv 8.7E-02 2
rs587777893
MTOR
0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs7094463
TCF7L2
10 112952224 intron variant A/G snv 0.57 1
rs34872471
TCF7L2
1.000 0.080 10 112994312 intron variant T/C snv 0.29 3
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
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
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs1427214163
TCF7L2
1.000 0.080 10 113151879 missense variant C/T snv 7.0E-06 2
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 5