Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 1
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 1
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7
rs11781551
LOC105375733
1.000 0.040 8 122395852 intergenic variant G/A snv 0.40 1
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 2
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 1
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 1
rs17045031
LOC105377142
1.000 0.040 3 66717940 intergenic variant G/A snv 0.10 1
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 1
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 1
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 1
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 2
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 1