Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 7
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs702553
PDE4D
0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs2075575
AQP4-AS1 ; AQP4
0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
rs3805435
GPX3 ; LOC105378228
0.882 0.120 5 151021735 non coding transcript exon variant T/C snv 8.4E-02 3
rs3736309
LOC101927318 ; AQP5 ; LOC105369764
0.925 0.120 12 49964271 intron variant A/G snv 0.12 2
rs3840634
CAV1
0.925 0.120 7 116556798 intron variant T/C snv 2
rs10489678
FCRL3
1.000 0.120 1 157699878 intron variant G/A;C;T snv 1
rs10955255
GRHL2
1.000 0.120 8 101524177 intron variant A/G;T snv 1
rs611419
LOC107986962 ; GRHL2 ; LOC107986961
1.000 0.120 8 101491489 intron variant T/A;C snv 1
rs6989650
GRHL2
1.000 0.120 8 101669109 3 prime UTR variant C/T snv 0.24 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs779829591
F3
0.827 0.320 1 94532395 missense variant G/A snv 4.0E-06 5
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs1264525329
SOD2
1.000 0.120 6 159682587 missense variant T/C snv 4.0E-06 1
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135