Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17197936 0.925 0.040 13 37601702 upstream gene variant T/C snv 5.2E-02 3
rs1385889785
FCRL3
1.000 0.040 1 157695436 missense variant G/C;T snv 4.0E-06; 4.0E-06 2
rs2165667
MTNR1A ; LOC105377596
0.925 0.040 4 186540475 intron variant A/G;T snv 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
rs4958847
IRGM
0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs10491322
PPP2CA
0.925 0.120 5 134194449 3 prime UTR variant A/G snv 9.5E-02 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
rs1477353313
ACR
0.925 0.120 22 50744085 missense variant T/G snv 2
rs1562444
MTNR1B
0.925 0.120 11 92982683 3 prime UTR variant G/A snv 0.55 2
rs204989
GPSM3
0.925 0.120 6 32194075 intron variant G/A snv 0.21 2
rs540558
OSMR ; OSMR-AS1
0.925 0.120 5 38844171 intron variant C/G snv 0.19 2
rs1057519090
COL4A2
0.851 0.160 13 110492105 missense variant G/A snv 7
rs771184127
NOD2
0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 9
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs741761
SEMA7A ; MIR6881
0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 3
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
rs28936375
CPT2
0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15