Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 7
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 6
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs2013002 12 111762346 intron variant T/A;C snv 5