Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 7
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs11749327
EXOC3
1.000 0.120 5 457146 non coding transcript exon variant C/A snv 0.20 2
rs1858800
ZFHX3
1.000 0.120 16 72990377 intron variant C/T snv 0.28 2
rs13124827 1.000 0.120 4 156419058 intergenic variant C/T snv 0.37 1
rs17208368 1.000 0.120 16 55038095 intergenic variant C/A snv 0.14 1
rs417096 1.000 0.120 6 39760057 intergenic variant G/A;C snv 0.53 1
rs4563609 1.000 0.120 5 158490267 intron variant G/A snv 0.73 1
rs6499755 0.925 0.120 16 55307223 intron variant T/C snv 0.30 1
rs7811653 1.000 0.120 7 46362671 intergenic variant C/A snv 5.8E-02 1
rs8045253 1.000 0.120 16 86404161 regulatory region variant T/C snv 0.33 1
rs988958 1.000 0.120 2 42060166 downstream gene variant G/A snv 0.25 1
rs17747401
ADK
1.000 0.120 10 74640406 intron variant C/T snv 0.27 1
rs17262815
CCDC26
1.000 0.120 8 129478919 intron variant T/C snv 0.13 1
rs143136847
CCDC59
1.000 0.120 12 82354560 missense variant T/C;G snv 2.6E-05; 2.8E-03 1
rs3812762
DENND2B
1.000 0.120 11 8730093 missense variant G/C snv 0.32 0.27 1
rs4554617
DGKK
0.925 0.120 X 50460404 intron variant A/C snv 0.45 1
rs1918690
DNAH6
1.000 0.120 2 84679791 intron variant T/C snv 0.74 1
rs2999052
EEFSEC
1.000 0.120 3 128173194 intron variant T/C snv 0.30 1
rs3743104
GREM1
1.000 0.120 15 32731784 3 prime UTR variant A/G;T snv 1
rs1801085
HOXA4 ; HOXA-AS2 ; HOXA3
1.000 0.120 7 27128971 splice region variant A/G snv 0.16 1
rs10762738
KCNMA1 ; KCNMA1-AS1
1.000 0.120 10 76935709 intron variant A/G snv 0.38 1
rs16937456
LOC105375894
1.000 0.120 8 71165720 intron variant A/G;T snv 1
rs3816183
MTA3 ; HAAO
0.925 0.120 2 42788579 missense variant T/C snv 0.80 0.80 1
rs10979
PHACTR2 ; PHACTR2-AS1
1.000 0.120 6 143568902 intron variant G/A snv 0.62 1