Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs1866389
THBS4
0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 9
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs771676129
CD36
0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 6
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 6
rs11234027
NADSYN1
0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs2149954
LINC02227
0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 5
rs3785889
GOSR2 ; LRRC37A2
0.827 0.080 17 46928464 intron variant G/A snv 0.45 5
rs6046
F7
0.925 0.080 13 113118845 missense variant G/A;C;T snv 0.13 5
rs756351287
PLA2G1B
0.827 0.080 12 120325936 missense variant G/A;C;T snv 2.4E-05 5
rs7692387
GUCY1A1
0.925 0.080 4 155714157 intron variant G/A snv 0.16 5
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 4
rs12762303
ALOX5
0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs1310478538
C3
0.851 0.080 19 6713295 missense variant C/G snv 1.4E-05 4
rs1333046
CDKN2B-AS1
0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs150629733
AGTR1
0.851 0.080 3 148741190 missense variant T/C;G snv 4.0E-06; 8.8E-05 4
rs1800576
THBD
0.925 0.080 20 23049378 missense variant C/T snv 2.0E-03 2.5E-03 4
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4