Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10491322
PPP2CA
0.925 0.120 5 134194449 3 prime UTR variant A/G snv 9.5E-02 3
rs540558
OSMR ; OSMR-AS1
0.925 0.120 5 38844171 intron variant C/G snv 0.19 2
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs204989
GPSM3
0.925 0.120 6 32194075 intron variant G/A snv 0.21 2
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
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
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
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
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
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13