Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10100465
LOC105375721
1.000 0.040 8 117614040 intergenic variant G/A snv 0.23 1
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 4
rs1040079
PACRG
0.882 0.040 6 162792995 intron variant A/G snv 0.31 3
rs10414149
SIGLEC5
1.000 0.040 19 51624491 intron variant A/G snv 0.30 1
rs1049432
TFAM
0.925 0.040 10 58395360 3 prime UTR variant G/C;T snv 2
rs10507522
LOC107984576
1.000 0.040 13 43904864 intron variant A/G snv 0.11 1
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs1071630
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
0.851 0.120 6 32641349 missense variant T/A;C snv 0.49 4
rs10817758
DELEC1
1.000 0.040 9 115381654 intron variant C/T snv 0.13 1
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs10982385 1.000 0.040 9 114730737 intergenic variant T/G snv 0.47 1
rs11003124
MBL2
1.000 0.040 10 52772131 upstream gene variant T/G snv 0.30 2
rs11174812
SLC2A13
1.000 0.040 12 40031285 intron variant C/T snv 0.36 1
rs11362
DEFB1
0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs12631031
PARL
0.925 0.040 3 183857982 intron variant G/A snv 0.12 2
rs13220141 1.000 0.040 6 146576497 intergenic variant A/T snv 8.2E-02 1
rs1333955
PACRG
0.851 0.080 6 162792422 intron variant T/A;C snv 4
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1554286
IL19 ; IL10
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs1587601 1.000 0.040 5 35254508 intergenic variant A/G snv 0.64 1
rs160451 1.000 0.040 8 89650713 intron variant T/C snv 0.56 1
rs16948876 1.000 0.040 16 50820507 intergenic variant G/A snv 6.2E-02 1
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47