Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs741761
SEMA7A ; MIR6881
0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 3
rs10911363
SMG7 ; NCF2
0.925 0.120 1 183580622 intron variant G/T snv 0.30 2
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1234315
TNFSF4
0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs11168268
VDR
0.925 0.120 12 47858029 intron variant G/A snv 0.57 2