Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 12
rs1740828 0.925 0.080 6 21648854 regulatory region variant G/A snv 0.55 2
rs605965 0.925 0.080 6 75723198 downstream gene variant T/A snv 2.3E-02 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1063539
ADIPOQ ; ADIPOQ-AS1
0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10 5
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1200003171
AKT1
0.882 0.120 14 104775122 missense variant C/A;T snv 8.0E-06 4
rs2494737
AKT1
0.925 0.080 14 104779988 intron variant T/A snv 0.40 2
rs2494750
AKT1
0.925 0.080 14 104796575 upstream gene variant G/C snv 0.86 2
rs72715985
AKT1
0.925 0.080 14 104797210 upstream gene variant C/T snv 2.6E-02 2
rs74090038
AKT1
0.925 0.080 14 104796444 upstream gene variant C/T snv 0.29 2
rs892119
AKT2 ; LOC107985289
0.925 0.080 19 40254165 intron variant C/T snv 0.19 2
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs1204038
AR
0.882 0.160 X 67568383 intron variant G/A snv 0.36 3
rs4987886
ATM
0.925 0.080 11 108225326 5 prime UTR variant A/T snv 3.0E-02 2
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs3768235
BCL10
0.925 0.080 1 85267691 missense variant C/T snv 8.0E-06; 6.5E-02 4.5E-02 2
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490