Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73115010
CD40
1.000 0.040 20 46124597 intron variant T/C snv 0.18 1
rs6074028
CD40
1.000 0.040 20 46126219 intron variant A/C;G snv 1
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs11168268
VDR
0.925 0.120 12 47858029 intron variant G/A snv 0.57 2
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
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
rs771184127
NOD2
0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 9
rs1477353313
ACR
0.925 0.120 22 50744085 missense variant T/G snv 2
rs28936375
CPT2
0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs12150220
NLRP1
0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs741761
SEMA7A ; MIR6881
0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 3
rs7033979
ASPN ; CENPP
0.925 0.040 9 92461698 intron variant A/G;T snv 2
rs1562444
MTNR1B
0.925 0.120 11 92982683 3 prime UTR variant G/A snv 0.55 2