Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs3115573 1.000 0.120 6 32251066 upstream gene variant A/G snv 0.41 2
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs4740
EBI3
0.827 0.240 19 4236999 missense variant G/A snv 0.34 0.39 8
rs9932581
MVD ; CYBA
16 88651945 3 prime UTR variant C/T snv 0.39 1
rs2281999
UNC13B
0.925 0.160 9 35381507 intron variant C/T snv 0.35 0.38 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs702553
PDE4D
0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs4309
ACE
0.925 0.120 17 63482562 synonymous variant C/T snv 0.46 0.36 3
rs3729548
SLC2A1
1.000 0.080 1 42934681 intron variant C/T snv 0.32 2
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs9275424 6 32702799 downstream gene variant A/G snv 0.30 1
rs3764880
TLR8-AS1 ; TLR8
0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs1883414
HLA-DPB2
0.925 0.200 6 33118671 non coding transcript exon variant G/A snv 0.28 3
rs6610650 1.000 0.040 X 37777261 intron variant G/A snv 0.27 2
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs37369
AGXT2
0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 9
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs74421874
PSMD9
0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10