Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs752596535
LDLR
0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs3751143
P2RX7 ; LOC105370032
0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs4717806
LOC105375350 ; STX1A ; BUD23
0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs33972313
SLC23A1
0.790 0.160 5 139379813 missense variant C/A;G;T snv 4.0E-06; 2.7E-02 8
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 3