Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048829
BMPR2
0.925 0.080 2 202565733 3 prime UTR variant T/A;G snv 4
rs10491678 1.000 0.040 9 29568688 intergenic variant T/A;C snv 1
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1051052
SERPINA1
1.000 0.040 14 94377595 3 prime UTR variant A/G snv 0.47 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 8
rs10519225
FGF7 ; FAM227B
1.000 0.040 15 49428581 intron variant G/A snv 0.28 1
rs10519717
LOC105377462
0.851 0.080 4 144559188 intron variant T/C snv 0.21 4
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1059823
SLC11A1
1.000 0.040 2 218395121 3 prime UTR variant A/G snv 0.52 1
rs1061581
HSPA1A ; HSPA1L
0.827 0.200 6 31816809 synonymous variant G/A snv 6
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 8
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs10760580 1.000 0.040 9 98899368 TF binding site variant G/A snv 0.22 1
rs10801558
CFH
1.000 0.040 1 196729914 intron variant T/G snv 0.46 2
rs10801559
CFH
1.000 0.040 1 196735074 intron variant G/A snv 0.44 2
rs1080879 1.000 0.040 5 15054693 intergenic variant T/C;G snv 1
rs10817688
DELEC1
1.000 0.040 9 114943689 intron variant A/G snv 0.39 2
rs10851906
IREB2
1.000 0.040 15 78482334 intron variant A/G snv 0.21 2
rs10866659
ADAM19
1.000 0.040 5 157510035 intron variant A/G;T snv 3
rs10873142
HIF1A ; HIF1A-AS3
1.000 0.040 14 61736744 intron variant C/T snv 0.67 1
rs10883944
STN1
1.000 0.040 10 103891899 intron variant G/T snv 0.31 2
rs10890311
RNF220
1.000 0.040 1 44602096 intron variant C/T snv 0.22 1