Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs2075575
AQP4-AS1 ; AQP4
0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
rs3840634
CAV1
0.925 0.120 7 116556798 intron variant T/C snv 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
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
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
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
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 7
rs7522061
FCRL3
0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 4
rs10489678
FCRL3
1.000 0.120 1 157699878 intron variant G/A;C;T snv 1
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs3805435
GPX3 ; LOC105378228
0.882 0.120 5 151021735 non coding transcript exon variant T/C snv 8.4E-02 3
rs10955255
GRHL2
1.000 0.120 8 101524177 intron variant A/G;T snv 1
rs6989650
GRHL2
1.000 0.120 8 101669109 3 prime UTR variant C/T snv 0.24 1
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92