Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs143383
GDF5
0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs110419
LOC105376536 ; LMO1
0.827 0.200 11 8231306 intron variant A/G snv 0.42 8
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs2011077
FGFR4
0.807 0.080 5 177094455 intron variant C/T snv 0.19 8