Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs1801280
NAT2
0.716 0.440 8 18400344 missense variant T/C snv 0.38 0.39 14
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs422951
NOTCH4
0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 8
rs4586
CCL2
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7
rs1816702
TLR2
0.827 0.120 4 153688371 non coding transcript exon variant T/C snv 0.79 6
rs11575934
IL12RB1
0.882 0.040 19 18075808 missense variant T/C snv 0.28 0.25 4
rs2071277
NOTCH4
0.882 0.200 6 32203906 intron variant T/C snv 0.48 0.46 3
rs4737420
LYN
0.925 0.080 8 55895622 non coding transcript exon variant T/C snv 0.38 3
rs11466617
TLR10
1.000 0.040 4 38778850 intron variant T/C snv 0.13 2
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs4958843
IRGM
0.925 0.080 5 150845362 upstream gene variant T/C snv 0.21 2
rs755850200
VDR
1.000 0.040 12 47846347 missense variant T/C snv 2.1E-05 7.0E-06 2
rs10051924
IRGM
1.000 0.040 5 150847077 5 prime UTR variant T/C snv 0.21 1
rs1059225
SFTPA1
1.000 0.040 10 79615230 3 prime UTR variant T/C snv 0.47 1
rs12294076
DYNC2H1
1.000 0.040 11 103256336 intron variant T/C snv 6.8E-02 1
rs17881720
SFTPA2
1.000 0.040 10 79555670 downstream gene variant T/C snv 6.7E-02 1
rs2543007
SLC14A2-AS1 ; SLC14A2
1.000 0.040 18 45471734 intron variant T/C snv 0.22 1
rs4736958
SFRP1
1.000 0.040 8 41261978 3 prime UTR variant T/C snv 3.6E-02 1
rs6114027
TGM6
1.000 0.040 20 2398952 intron variant T/C snv 0.15 1
rs6676375 1.000 0.040 1 242711583 intergenic variant T/C snv 0.15 1
rs549908
IL18
0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs4129009
TLR10
0.882 0.120 4 38773268 missense variant T/A;C;G snv 0.17 0.13 6