Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 7
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 7
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 6
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 6
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 6
rs2306235
PLEKHO1
0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 5
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 5
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5