Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1085308051
PTEN
0.882 0.200 10 87933229 missense variant A/G snv 4.0E-06 6
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs888208
NKX2-3
0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25 3
rs10491434
IL7R
1.000 0.080 5 35877812 3 prime UTR variant A/G snv 0.32 2
rs212400
LOC105378083
0.925 0.200 6 159052542 non coding transcript exon variant A/G snv 0.64 2
rs936229
ULK3
1.000 0.080 15 74839978 intron variant A/G snv 0.67 2
rs182429
LOC107986664 ; LOC105378083
1.000 0.080 6 159048542 intron variant A/G snv 0.49 1
rs4897233
THEMIS
1.000 0.080 6 127835743 intron variant A/G snv 0.38 1
rs6715106
STAT4
1.000 0.080 2 191048308 intron variant A/G snv 6.1E-02 1
rs6752770
STAT4
1.000 0.080 2 191108837 intron variant A/G snv 0.31 1
rs79758729
ELMO1
1.000 0.080 7 37378851 intron variant A/G snv 7.9E-02 1
rs8081319
ACACA ; C17orf78
1.000 0.080 17 37374139 intron variant A/G snv 6.8E-02 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs17264332 0.925 0.200 6 137684378 intron variant A/G;T snv 2
rs531930
NKAIN2
1.000 0.080 6 124422361 intron variant A/G;T snv 1
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs6432714
IFIH1
0.882 0.160 2 162280842 intron variant A/T snv 0.16 3
rs10203477
LINC01185
0.925 0.200 2 60877850 intron variant A/T snv 0.48 2