Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3130361 0.925 0.160 6 30371787 intergenic variant A/G snv 0.81 3
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs6489956
TBX5
1.000 0.040 12 114354431 3 prime UTR variant T/C snv 0.80 1
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs510317
F7
1.000 0.040 13 113105440 upstream gene variant A/G;T snv 0.79 1
rs4665630
KLHL29
0.925 0.080 2 23675447 intron variant C/T snv 0.78 3
rs428785
ADAMTS1
0.882 0.040 21 26844276 missense variant C/A;G;T snv 1.3E-05; 0.70 0.78 3
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs180070
LINC01497
0.882 0.040 17 69960745 upstream gene variant G/T snv 0.77 4
rs383830 0.882 0.040 5 100613278 intergenic variant A/T snv 0.76 3
rs1549758
NOS3
0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs3740107
ALOX5
1.000 0.040 10 45428322 intron variant A/G snv 0.76 1
rs1153188 0.925 0.120 12 54705212 intergenic variant T/A snv 0.76 2
rs4143832 0.925 0.080 5 132527285 intron variant T/G snv 0.76 4
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5
rs2740483
ABCA1 ; LOC105376196
0.882 0.120 9 104928254 intron variant G/C snv 0.75 3
rs7961581
TSPAN8
0.827 0.200 12 71269322 intron variant C/T snv 0.75 7
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 9