Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs1800875
CMA1
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
rs762513613
FCGR2C
0.752 0.280 1 161591315 missense variant A/G snv 4.2E-06 7.4E-06 11
rs3740360
PLCE1
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs3132468
MICB
0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
rs5745568
GGNBP1 ; BAK1
0.882 0.080 6 33580617 intron variant G/T snv 0.19 4
rs750898115
USO1
0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 4
rs1285933
CLEC5A ; MGAM
0.925 0.040 7 141927349 intron variant G/A snv 0.54 2
rs1447043692
HPSE2
0.925 0.040 10 98641918 missense variant C/T snv 2
rs3739319
IDO1
0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 2
rs371057322
KIDINS220
0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 2
rs6500818
RBFOX1
0.925 0.040 16 6767374 intron variant C/T snv 0.11 2
rs10104997
RP1
0.925 0.040 8 54527508 intron variant C/T snv 0.19 2
rs4973
ACE
1.000 0.040 17 63486691 synonymous variant A/G snv 1
rs1317403430
CFH
1.000 0.040 1 196673869 missense variant G/A snv 4.0E-06 1
rs2780831
JAK1
1.000 0.040 1 64880504 intron variant C/T snv 0.35 1