Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs587777893
MTOR
0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs3811463
LIN28A
0.752 0.400 1 26427451 3 prime UTR variant T/A;C snv 14
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs10923931
NOTCH2
0.925 0.120 1 119975336 intron variant G/T snv 0.17 3
rs945508
ARHGEF11 ; MIR765 ; LRRC71
1.000 0.080 1 156937289 missense variant T/C snv 0.64 0.66 3
rs1042842
MFN2
1 12011623 3 prime UTR variant A/G snv 0.71 1
rs10802502
NLRP3
1 247448993 3 prime UTR variant C/T snv 0.55 1
rs17429130
RXRG
1 165401015 3 prime UTR variant G/C snv 4.2E-02 1
rs909221872
ACOT7
1 6349856 missense variant G/T snv 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
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
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18