Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs11207997
DOCK7 ; ANGPTL3
1 62596235 intron variant C/T snv 0.39 5
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 5
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs1748197
DOCK7
1 62590441 intron variant G/A snv 0.42 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2131925
DOCK7
1 62560271 intron variant G/T snv 0.57 5
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 5
rs9436735
LEPR ; LEPROT
1 65419378 upstream gene variant C/G snv 2.5E-02 5
rs11465759
IL23R ; C1orf141
1 67166721 intron variant T/G snv 2.4E-02 4
rs11571111
REN
1 204161105 intron variant C/A snv 5.0E-03 4
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 4
rs1277930
PSRC1
1 109279521 downstream gene variant G/A snv 0.63 4
rs567279
PDE4B
1 66222346 intron variant G/T snv 0.97 4