Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10930328
CERS6
0.925 0.040 2 168522904 intron variant T/G snv 0.18 2
rs10959745
LOC105375974
0.925 0.040 9 11366989 intron variant T/G snv 8.9E-02 2
rs11139622
LOC105376110 ; LOC107987087
0.925 0.040 9 82569420 intron variant T/G snv 6.1E-02 2
rs11178610 0.925 0.040 12 71105594 intron variant T/G snv 1.9E-03 2
rs11219814 0.925 0.040 11 124858227 intergenic variant T/G snv 0.18 2
rs11997538
LOC107986943
0.925 0.040 8 52920103 intergenic variant T/G snv 0.18 2
rs12086567
LOC105373108
0.925 0.040 1 224811130 intron variant T/G snv 0.12 2
rs1517284
ABCC9
0.925 0.040 12 21835154 intron variant T/G snv 0.12 2
rs1655098 0.925 0.040 10 130924740 intergenic variant T/G snv 0.91 2
rs16966555 0.925 0.040 16 63768670 intergenic variant T/G snv 6.0E-02 2
rs17032384
LINC02456 ; HELLPAR
0.925 0.040 12 102283136 non coding transcript exon variant T/G snv 3.9E-02 2
rs17046259
MSMO1
0.925 0.040 4 165338567 intron variant T/G snv 0.10 2
rs17166189
SCIN ; LOC107986769
0.925 0.040 7 12579299 intron variant T/G snv 3.9E-02 2
rs17768858
CHODL
0.925 0.040 21 17960675 intron variant T/G snv 3.1E-02 2
rs1814813
KLHL2P1
0.925 0.040 4 119337052 intron variant T/G snv 0.37 2
rs2124373
HPS5
0.925 0.040 11 18292190 intron variant T/G snv 3.1E-02 2
rs2830622
LOC112268279
0.925 0.040 21 27014343 intergenic variant T/G snv 0.20 2
rs2832402
GRIK1 ; BACH1
0.925 0.040 21 29580346 intron variant T/G snv 2.7E-02 2
rs2870831 0.925 0.040 12 68989056 intergenic variant T/G snv 0.91 2
rs3011823 0.925 0.040 6 82442503 regulatory region variant T/G snv 1.8E-03 2
rs3899582
MTUS2
0.882 0.120 13 29003859 intron variant T/G snv 1.9E-02 2
rs41439051
RIT2
0.925 0.040 18 42940094 intron variant T/G snv 3.4E-02 2
rs4627442
FHOD3
0.925 0.040 18 36336269 intron variant T/G snv 0.14 2
rs4762293
ELK3
0.925 0.040 12 96261458 intron variant T/G snv 0.22 2
rs663599
LATS2
0.925 0.040 13 20984315 intron variant T/G snv 0.83 2