Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 4
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs1892534
LEPR
0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 3
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs661955 1 234707109 upstream gene variant G/C;T snv 3
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 3
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs11208722 1 65705318 intron variant C/A snv 0.75 2
rs1127311
ADAR ; CHRNB2
1 154584187 3 prime UTR variant G/A snv 0.42 2
rs11573156
PLA2G2A
0.882 0.240 1 19979653 5 prime UTR variant G/C snv 0.19 2
rs12068753 1.000 0.120 1 159722747 intergenic variant T/A snv 0.15 2
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 2
rs12742376
KDF1
1 26958704 intron variant C/T snv 6.8E-02 2
rs12755606 1 159700546 downstream gene variant C/G snv 0.24 2
rs17519972
GLMN ; RPAP2
1.000 0.080 1 92362948 intron variant A/C snv 0.15 2
rs17597773
HLX-AS1 ; HLX
1 220881419 non coding transcript exon variant C/G snv 0.25 0.23 2
rs2307246
PLA2G2A
1 19978364 non coding transcript exon variant G/A snv 0.18 0.18 2
rs2592902 1.000 0.080 1 159685936 intergenic variant G/A;T snv 0.35 2