Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 3
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs17037390
MTHFR
1.000 0.040 1 11800786 non coding transcript exon variant G/A snv 0.18 3
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 3
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 3
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 3
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 2
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 2
rs17114046
PLPP3
0.925 0.040 1 56500678 intron variant A/G snv 0.12 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 2