Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 4
rs6437061
DIS3L2
2 232320342 intron variant A/C snv 0.56 3
rs12854631 X 58297412 intergenic variant A/C snv 2.7E-02 2
rs139214349 4 29168543 intron variant A/C snv 1.4E-02 2
rs147168872
SOS2
14 50173277 intron variant A/C snv 5.0E-03 2
rs1856293 6 133159801 intergenic variant A/C snv 0.56 2
rs2656052
IREB2
15 78448590 intron variant A/C snv 0.36 2
rs72724928
LINGO2
9 28024196 intron variant A/C snv 3.3E-02 2
rs72923818
DYM
18 49157384 intron variant A/C snv 4.0E-02 2
rs11072811
MORF4L1
1.000 0.040 15 78839988 intron variant A/C snv 0.51 1
rs6495314
CHRNB4 ; LOC112268142
0.925 0.080 15 78668187 intron variant A/C snv 0.35 1
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs4947642 7 51797912 intergenic variant A/C;G snv 3
rs6090583
EYA2
20 46930192 intron variant A/C;G snv 3
rs189798510 17 14811500 intergenic variant A/C;G snv 2
rs2945731 8 133627845 intergenic variant A/C;G snv 4.9E-02 2
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 3
rs7773004 1.000 0.040 6 26267527 downstream gene variant A/C;G;T snv 3
rs12903295
IREB2
15 78486630 intron variant A/C;G;T snv 2
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs148215758
PHF8
X 54017674 synonymous variant A/C;T snv 2.6E-02 2
rs6470765
GSDMC
8 129724451 upstream gene variant A/C;T snv 2
rs8042059
CHRNA3
0.882 0.080 15 78615517 intron variant A/C;T snv 2