Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs2275725
ADAM8
1.000 0.080 10 133275531 missense variant A/G snv 0.89 0.90 1
rs6809699
P2RY12 ; MED12L
1.000 0.080 3 151338810 synonymous variant A/C snv 0.87 0.88 2
rs670950
KCNN4
1.000 0.080 19 43777410 intron variant T/C snv 0.87 1
rs824400
OSGIN1
1.000 0.080 16 83956331 intron variant C/G snv 0.85 1
rs2302685
BCL2L14 ; LRP6
0.827 0.240 12 12148964 missense variant C/T snv 0.85 0.84 5
rs2995300
ADAM8
1.000 0.080 10 133263019 3 prime UTR variant C/A snv 0.87 0.83 1
rs1613662
GP6 ; LOC107985325
0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs562556
PCSK9
0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 8
rs10733113 0.882 0.160 1 247459055 upstream gene 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
rs2073746
ARVCF
1.000 0.080 22 19991035 intron variant T/C snv 0.80 1
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs14309
RNASEK-C17orf49 ; C17orf49 ; MIR497HG
1.000 0.080 17 7015774 splice region variant T/C snv 0.80 0.76 1
rs1319501
NAMPT
0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 4
rs6003
F13B
0.851 0.240 1 197061891 missense variant C/T snv 0.88 0.76 5
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 5
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs1234313
TNFSF4
0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140