Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs11225138
YAP1
0.925 0.200 11 102123167 intron variant G/C snv 6.1E-02 2
rs11225154
YAP1
1.000 0.120 11 102172509 intron variant G/A;C snv 1
rs11225161
YAP1
1.000 0.120 11 102199763 intron variant C/T snv 7.0E-02 1
rs1894116
YAP1
1.000 0.120 11 102199908 intron variant A/G snv 8.2E-02 1
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs34911341
GHRL ; GHRLOS
0.882 0.200 3 10289835 missense variant C/T snv 7.0E-03 7.3E-03 5
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 7
rs11212617
C11orf65
0.827 0.200 11 108412434 intron variant C/A snv 0.49 7
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
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
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 5
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs11196218
TCF7L2
0.925 0.160 10 113080735 intron variant G/A snv 0.25 2
rs11196229
TCF7L2
0.925 0.160 10 113106413 intron variant G/A snv 0.19 2
rs11196236
TCF7L2
0.925 0.160 10 113127963 intron variant T/C snv 0.16 2
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs1784692
ZBTB16
1.000 0.120 11 114078510 intron variant T/C snv 0.17 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs363282
PDZD8 ; SLC18A2
1.000 0.120 10 117278157 3 prime UTR variant G/A snv 0.77 1
rs363238
PDZD8 ; SLC18A2
1.000 0.120 10 117279248 3 prime UTR variant C/A snv 0.14 1
rs804279 1.000 0.120 8 11766380 upstream gene variant A/T snv 0.72 1