Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5
rs1364989 0.925 0.160 4 54145602 intron variant T/C snv 0.73 2
rs601162 0.925 0.160 9 29632144 upstream gene variant A/C;G;T snv 2
rs6697139 0.925 0.160 1 161690906 intergenic variant G/A;T snv 2
rs7692514 0.925 0.160 4 65276878 intergenic variant G/A;C snv 2
rs7773456 0.925 0.160 6 19823007 intron variant T/G snv 0.35 2
rs17008504 1.000 0.160 4 124718662 intergenic variant T/A snv 4.3E-02 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2271100
AGA
1.000 0.160 4 177438525 intron variant T/C snv 0.19 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs172378
C1QA
0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs1108131
CAMK1D
0.925 0.160 10 12455748 intron variant T/C snv 0.28 2
rs2246614
CDHR5
0.882 0.160 11 619789 missense variant T/G snv 0.63 0.59 3
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs2295415
CREM
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19 3
rs2298804
FCER1A
0.851 0.240 1 159304102 missense variant A/G;T snv 6.6E-03 4
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12