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
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs7961581
TSPAN8
0.827 0.200 12 71269322 intron variant C/T snv 0.75 7
rs712699
PAX4
7 127610543 3 prime UTR variant G/A snv 0.75 1
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1042842
MFN2
1 12011623 3 prime UTR variant A/G snv 0.71 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs945508
ARHGEF11 ; MIR765 ; LRRC71
1.000 0.080 1 156937289 missense variant T/C snv 0.64 0.66 3
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs7178572
HMG20A
0.925 0.120 15 77454848 intron variant A/G snv 0.63 3
rs4746822
LOC101928994 ; HKDC1
10 69223185 non coding transcript exon variant C/T snv 0.59 2
rs10762264
LOC101928994
10 69217077 intron variant G/A snv 0.58 1
rs391300
SRR
0.882 0.160 17 2312964 intron variant T/C snv 0.58 4
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2119882
MTNR1A
0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9