Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs997509
ENPP1
0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28 5
rs13038305
CST3
0.925 0.080 20 23629625 intron variant C/T snv 0.21 5
rs1414334
HTR2C
0.851 0.160 X 114903581 intron variant C/G snv 5
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs1554483
CLOCK
0.882 0.160 4 55455650 intron variant C/G snv 0.33 5
rs2144908
LOC105372629 ; HNF4A
0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs2267443
SREBF2
0.882 0.120 22 41891450 intron variant A/G snv 0.67 5
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 5
rs6454674
CNR1
0.851 0.120 6 88163211 intron variant T/G snv 0.32 5
rs8057044
FTO
0.882 0.080 16 53778702 intron variant G/A snv 0.54 5
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 4
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 4
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37 4
rs16940212
ALDH1A2
1.000 0.040 15 58401821 intron variant G/A;T snv 4
rs17276588
MIRLET7F2 ; MIR98 ; HUWE1
0.882 0.120 X 53557457 intron variant G/A snv 9.0E-02 4.2E-02 4
rs1884051
ESR1
0.882 0.080 6 151962144 intron variant G/A snv 0.60 4
rs2199503
GSK3B
0.851 0.080 3 120059642 intron variant T/C snv 0.79 4
rs2206277
TFAP2B
0.925 0.080 6 50830813 intron variant C/T snv 0.19 4
rs2250656
C3
0.882 0.160 19 6718523 intron variant T/C snv 0.25 4
rs2544390
LRP2
0.925 0.080 2 169348336 intron variant C/T snv 0.45 4
rs263
LPL
1.000 0.040 8 19955301 intron variant C/T snv 0.23 4