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
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2165667
MTNR1A ; LOC105377596
0.925 0.040 4 186540475 intron variant A/G;T snv 2
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
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
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs28936375
CPT2
0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs3789604
RSBN1 ; AP4B1-AS1
0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7
rs1234315
TNFSF4
0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs10911363
SMG7 ; NCF2
0.925 0.120 1 183580622 intron variant G/T snv 0.30 2
rs1385889785
FCRL3
1.000 0.040 1 157695436 missense variant G/C;T snv 4.0E-06; 4.0E-06 2