Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
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
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
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
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs4958847
IRGM
0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs1057519090
COL4A2
0.851 0.160 13 110492105 missense variant G/A snv 7
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
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
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
rs10491322
PPP2CA
0.925 0.120 5 134194449 3 prime UTR variant A/G snv 9.5E-02 3
rs17197936 0.925 0.040 13 37601702 upstream gene variant T/C snv 5.2E-02 3
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3