Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5369
EDN1
1.000 0.120 6 12294025 synonymous variant A/G snv 0.90 0.88 1
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 5
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs5070
APOA1 ; APOA1-AS
0.882 0.160 11 116837304 intron variant A/G snv 0.56 0.60 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs243327
RMI2 ; LOC105371082
0.882 0.280 16 11259447 intron variant A/G snv 0.52 4
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs4783961
CETP
0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 7
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17