Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs997506328
ERI2
1.000 0.080 16 20799983 missense variant A/G snv 1
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs995343
SLC16A7
0.925 0.120 12 59685594 intron variant G/A snv 0.57 2
rs9944880
DCC
0.882 0.120 18 53125996 intron variant G/A snv 5.3E-02 3
rs994308 0.776 0.080 20 6622975 intergenic variant C/T snv 0.43 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9939049
CDH1
0.790 0.080 16 68778398 intron variant A/T snv 0.29 9
rs9930005 0.776 0.080 16 80009361 intergenic variant C/A;T snv 10
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 16
rs9924886
CDH3
0.776 0.080 16 68710036 intron variant A/C snv 0.25 10
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 10
rs9921222
AXIN1
0.925 0.120 16 325782 intron variant C/T snv 0.51 5
rs9912300
ACLY
0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78 5
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs9901225
RETREG3
0.790 0.080 17 42603793 intron variant C/G;T snv 10
rs990101456
LDB1
1.000 0.080 10 102109138 missense variant C/T snv 1
rs989902
PTPN13
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs9858822
PPARG
0.925 0.080 3 12369739 intron variant A/C snv 0.11 2
rs984907158
FBXO11 ; MSH6
0.925 0.080 2 47799048 synonymous variant T/C snv 4.0E-06 2.8E-05 2
rs9834244 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 10
rs983402 0.776 0.080 2 198916862 intron variant T/C snv 0.62 10
rs983318
LINC00511 ; LINC00673
0.776 0.080 17 72417112 intron variant G/A snv 0.18 10
rs9831861 0.790 0.080 3 53054269 intron variant T/G snv 0.53 9
rs982873 0.925 0.160 13 90145678 intergenic variant T/C snv 0.65 2
rs980578884
POLE
0.925 0.080 12 132673217 missense variant C/T snv 1.4E-05 2