Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs25648
VEGFA
0.742 0.320 6 43771240 synonymous variant C/G;T snv 8.5E-06; 0.16 11
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 10
rs549908
IL18
0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 8
rs3755724
TIMP4 ; SYN2
0.790 0.360 3 12159406 intron variant C/T snv 0.31 8
rs4523
TBXA2R
0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66 8
rs7305115
TPH2
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 7
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs738792
MMP11
0.827 0.240 22 23779191 missense variant C/T snv 0.84 0.80 6
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs1600249
BLK
0.827 0.280 8 11502129 intron variant G/T snv 0.23 5
rs2070676
CYP2E1
0.827 0.320 10 133537633 non coding transcript exon variant G/C snv 0.73 5
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 5
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 5
rs113420705
CASP3 ; PRIMPOL
0.925 0.160 4 184649399 5 prime UTR variant T/C snv 0.31 4
rs1861493
IFNG ; IFNG-AS1
0.851 0.280 12 68157416 intron variant G/A snv 0.76 4
rs2229634
ITPR3
0.851 0.240 6 33670403 synonymous variant C/A;T snv 4.0E-06; 0.33 4
rs2254556 0.851 0.280 6 31374854 intron variant T/C snv 0.85 4
rs4840568
BLK
0.882 0.160 8 11493510 intron variant G/A snv 0.32 4