Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs4958847
IRGM
0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
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
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs10911363
SMG7 ; NCF2
0.925 0.120 1 183580622 intron variant G/T snv 0.30 2
rs11168268
VDR
0.925 0.120 12 47858029 intron variant G/A snv 0.57 2
rs204989
GPSM3
0.925 0.120 6 32194075 intron variant G/A snv 0.21 2
rs2165667
MTNR1A ; LOC105377596
0.925 0.040 4 186540475 intron variant A/G;T snv 2
rs540558
OSMR ; OSMR-AS1
0.925 0.120 5 38844171 intron variant C/G snv 0.19 2
rs7033979
ASPN ; CENPP
0.925 0.040 9 92461698 intron variant A/G;T snv 2
rs6074028
CD40
1.000 0.040 20 46126219 intron variant A/C;G snv 1
rs73115010
CD40
1.000 0.040 20 46124597 intron variant T/C snv 0.18 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306