Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs1256049
ESR2
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs7833904 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 3
rs767523236
MPO
0.925 0.040 17 58279033 missense variant T/C snv 4.1E-06 7.0E-06 2
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs569033466
CETP
0.882 0.160 16 56961929 5 prime UTR variant G/A;C;T snv 4.8E-05; 2.4E-05 6
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 9
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 6