Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs1554286
IL19 ; IL10
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs3753395
CFH
0.882 0.120 1 196717522 intron variant A/G;T snv 5
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 4
rs1071630
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
0.851 0.120 6 32641349 missense variant T/A;C snv 0.49 4
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs1333955
PACRG
0.851 0.080 6 162792422 intron variant T/A;C snv 4
rs730880295
LACC1
0.851 0.200 13 43883879 missense variant T/C snv 4
rs2844573 0.882 0.160 6 31367677 intron variant A/C;G snv 3
rs1049432
TFAM
0.925 0.040 10 58395360 3 prime UTR variant G/C;T snv 2
rs2270368
SNX20
0.925 0.080 16 50680424 intron variant G/A;C snv 2
rs7298930
LRRK2
0.925 0.040 12 40325698 intron variant A/C;G;T snv 2
rs9271100
HLA-DRB1
0.925 0.120 6 32608701 regulatory region variant T/A;C snv 2
rs2024825
C1orf141
1.000 0.040 1 67132294 intron variant T/A;C;G snv 1
rs2221593
BATF3
1.000 0.040 1 212700089 upstream gene variant C/A;G;T snv 1
rs2524132
LINC02571 ; HLA-B ; LOC112267902
1.000 0.040 6 31297135 intron variant G/A;T snv 1
rs3088362
CCDC122
1.000 0.040 13 43859494 intron variant C/A;T snv 1
rs34411505 1.000 0.040 16 27395368 intergenic variant A/C;G snv 1
rs4720118
BBS9
1.000 0.040 7 33429629 intron variant T/A;C snv 1
rs55894533 1.000 0.040 8 11891733 downstream gene variant A/C;T snv 1
rs58744688
FMNL1
1.000 0.040 17 45230816 intron variant A/C;G snv 1