Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs2227981
LOC105373977 ; PDCD1
0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12
rs25648
VEGFA
0.742 0.320 6 43771240 synonymous variant C/G;T snv 8.5E-06; 0.16 11
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 10
rs549908
IL18
0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs7305115
TPH2
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs2229634
ITPR3
0.851 0.240 6 33670403 synonymous variant C/A;T snv 4.0E-06; 0.33 4
rs28493229
ITPKC ; COQ8B
0.925 0.200 19 40718299 intron variant G/A;C snv 6.0E-06; 0.12 3
rs7637803
MED12L ; P2RY12
0.882 0.160 3 151371438 intron variant C/G;T snv 3
rs7849782
GRIN3A
0.925 0.160 9 101664982 intron variant C/A;G;T snv 3
rs11793049
ZNF618
0.925 0.120 9 114011589 intron variant A/G;T snv 2
rs1382568
BLK
0.925 0.160 8 11493711 intron variant A/C;G snv 2
rs1561876
STIM1
0.925 0.160 11 4092165 3 prime UTR variant G/A;C;T snv 2
rs1564267 0.925 0.160 8 11480378 non coding transcript exon variant T/A;C;G snv 2
rs2409781
BLK
0.925 0.120 8 11502048 intron variant T/A;C snv 2
rs2618444 0.925 0.160 8 11480861 intron variant A/C;T snv 2
rs2736332 0.925 0.160 8 11482456 upstream gene variant G/C;T snv 2