Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9298814
IFNA17
0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7
rs10766197
CYP2R1
0.807 0.240 11 14900334 upstream gene variant G/A;C snv 6
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs3731865
SLC11A1
0.882 0.160 2 218385280 non coding transcript exon variant G/A;C;T snv 0.23; 1.4E-04 5
rs11045819
SLCO1B1
0.851 0.120 12 21176879 missense variant C/A;T snv 0.11; 4.0E-06 4
rs2723176
IL37
0.851 0.200 2 112914932 intron variant A/C;G snv 4
rs3242
SFRP1
0.851 0.160 8 41262035 3 prime UTR variant G/A;C snv 4
rs8177400
TIRAP
0.882 0.160 11 126292695 missense variant G/A;C;T snv 2.8E-03; 1.2E-05 4
rs1131454
OAS1
0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs1405655
NR1H2
0.925 0.120 19 50379362 intron variant T/C;G snv 3
rs3809849
MYBBP1A
0.882 0.120 17 4555303 missense variant G/C;T snv 0.21; 3.1E-05 3
rs386699558
LOC107986589 ; HLA-DQA1 ; HLA-DQA2
0.882 0.080 6 32642624 missense variant GCC/ACA mnv 3
rs3923647
TLR1
0.925 0.080 4 38797918 missense variant T/A;C;G snv 2.7E-02; 4.0E-06; 1.6E-05 3
rs7749390
IFNGR1
0.882 0.120 6 137219233 5 prime UTR variant A/G;T snv 0.43; 4.4E-06 3
rs1052632
MR1
0.925 0.080 1 181051094 non coding transcript exon variant G/A;C snv 2
rs1344800847
CR1
0.925 0.120 1 207569911 missense variant G/T snv 2
rs1474798132
ZSCAN25 ; CYP3A5
0.925 0.120 7 99665170 synonymous variant T/A;C snv 4.0E-06; 4.0E-06 2
rs1650232
SFTPA2
1.000 0.040 10 79559511 splice region variant C/A;T snv 3.6E-03; 0.71 2
rs2248949
NR1H2
0.925 0.120 19 50378912 non coding transcript exon variant A/G;T snv 2
rs34448891
SLC11A1
0.925 0.160 2 218381927 upstream gene variant TGTGTGTG/-;TG;TGTG;TGTGTG;TGTGTGTGTG;TGTGTGTGTGTG;TGTGTGTGTGTGTG;TGTGTGTGTGTGTGTG delins 2
rs35037722 0.925 0.040 17 78355453 upstream gene variant G/A;C snv 2
rs3738467
CR1
0.925 0.120 1 207552816 missense variant G/T snv 1.4E-03 2
rs3758673
NR1H3
0.925 0.120 11 47257366 intron variant C/G;T snv 2
rs401502
IL12RB1
0.925 0.040 19 18069603 missense variant C/A;G;T snv 0.28; 3.2E-05 2