Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1013579
C8B
1 56956811 missense variant C/T snv 0.98 0.98 1
rs6472812
LY96
1.000 0.080 8 74004849 missense variant A/G snv 0.97 0.97 2
rs908830
C8G ; FBXW5
9 136946407 intron variant T/C snv 0.96 0.95 1
rs4725617
EPHA1
7 143400007 missense variant A/G;T snv 0.93 1
rs808919
ANKRD52
12 56254127 synonymous variant G/C;T snv 0.91; 2.4E-05 1
rs611779
ADGRF5
6 46859173 synonymous variant G/A;T snv 0.91 1
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs4546904
PTGFRN
1 116945089 missense variant T/A snv 0.89; 2.8E-05; 8.1E-06 0.87 1
rs217116
CTSC
11 88300493 intron variant A/C;G;T snv 0.88; 8.0E-06 1
rs5757973
IGLV1-47
22 22358119 missense variant T/A;C;G snv 1.2E-05; 0.88 1
rs2250889
SLC12A5-AS1 ; MMP9
0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs1654425
GP6 ; LOC107985325
19 55027612 synonymous variant T/C;G snv 0.87; 4.0E-05 1
rs2016575
LOC105377091 ; SEMA3G
3 52443064 missense variant T/C snv 0.86 0.81 1
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs28480494
APOL1
22 36265106 intron variant G/A;C;T snv 0.83; 4.1E-06 1
rs28361034
CYP21A2 ; CYP21A1P
6 32006946 intron variant A/C;G;T snv 6.3E-06; 0.83; 2.5E-05 1
rs812936
FUT3
1.000 0.080 19 5844638 missense variant G/A;C snv 0.83 2
rs941923
WARS1
14 100346740 splice region variant T/C snv 0.76 0.69 1
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs8192917
LOC107984667 ; GZMB
0.925 0.040 14 24632954 missense variant C/T snv 0.76 0.72 3
rs693698
LBHD1 ; UQCC3
11 62671347 5 prime UTR variant G/A;T snv 0.75 1
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs3865014
GLCE
0.851 0.080 15 69269179 missense variant G/A snv 0.75 0.69 8
rs1926447
CPB2 ; CPB2-AS1
0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs1926446
CPB2-AS1 ; CPB2
13 46055860 intron variant C/A;G snv 0.73 1