Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs17879469
HLA-DRB1
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs11611206
LOC105369818 ; MDM1
0.851 0.200 12 68274666 intron variant G/A snv 0.15 4
rs11250144
BLK
0.925 0.200 8 11528767 intron variant G/A;C snv 2
rs376511
IL17RC
1.000 0.040 3 9921132 intron variant A/G;T snv 1
rs10178082
MGC4859 ; LOC107986766
1.000 0.040 7 10667285 intron variant T/A snv 1