Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11099680
NR3C2
1.000 0.040 4 148182095 intron variant G/A snv 0.78 2
rs928940
IL1RN
0.882 0.120 2 113119918 intron variant G/T snv 0.78 3
rs743507
NOS3
0.882 0.200 7 151010400 intron variant C/T snv 0.77 4
rs3937443
POU6F2 ; LOC105375238
1.000 0.040 7 39474399 intron variant T/C snv 0.77 2
rs1549758
NOS3
0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs4965373
SELENOS
1.000 0.040 15 101272190 non coding transcript exon variant A/G snv 0.74 1
rs2604204
KCNJ5
0.882 0.120 11 128917535 3 prime UTR variant G/T snv 0.74 3
rs569805
ABCB11
1.000 0.040 2 168926370 intron variant A/T snv 0.73 2
rs496300
LINC01679
1.000 0.040 21 43359800 intron variant C/T snv 0.73 2
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs180088 1.000 0.040 17 69951455 intergenic variant T/A;C 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
rs7566605
LOC107985940
0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs4917
AHSG
0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 9
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1801704
ADRB2
0.882 0.200 5 148826812 5 prime UTR variant C/T snv 0.68 0.68 3