Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10955255
GRHL2
1.000 0.120 8 101524177 intron variant A/G;T snv 1
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1264525329
SOD2
1.000 0.120 6 159682587 missense variant T/C snv 4.0E-06 1
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2075575
AQP4-AS1 ; AQP4
0.851 0.200 18 26866562 intron variant G/A snv 0.31 5
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs3736309
LOC101927318 ; AQP5 ; LOC105369764
0.925 0.120 12 49964271 intron variant A/G snv 0.12 2
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 7
rs3805435
GPX3 ; LOC105378228
0.882 0.120 5 151021735 non coding transcript exon variant T/C snv 8.4E-02 3
rs3840634
CAV1
0.925 0.120 7 116556798 intron variant T/C snv 2
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99