Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs8089
LOC101929523 ; THBS2
0.851 0.080 6 169217631 splice region variant A/C snv 0.22 4
rs8075977 0.827 0.160 17 1757507 upstream gene variant T/C snv 0.37 5
rs805296
BAG6 ; APOM
0.851 0.120 6 31655116 intron variant T/A;C snv 4
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs778916575
CAD
0.882 0.040 2 27222595 missense variant G/A snv 1.2E-05 3
rs77832441
CRP
0.882 0.040 1 159714024 missense variant G/A snv 1.4E-03 1.6E-03 3
rs775381348
PSMA6
0.807 0.160 14 35308023 missense variant G/T snv 8
rs774695111
CYP2C8
0.882 0.040 10 95069271 missense variant C/A snv 4.0E-06 3
rs774232279
LIPC
0.882 0.040 15 58548572 missense variant G/A;T snv 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs772132247
LPL
0.882 0.040 8 19959292 missense variant G/A snv 5.2E-05 7.0E-06 3
rs771676129
CD36
0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs770572030
LIPG
0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 5
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs765798193
PSMD9
0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs763802417
NOX1
0.882 0.040 X 100862805 missense variant G/A snv 5.9E-06 5