Source: GWASDB ×
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 24
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 5
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 4
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 4
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 4
rs11953630 5 158418394 intergenic variant C/A;T snv 3
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 3
rs4373814 10 18131043 intergenic variant G/C;T snv 3
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 3
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 3
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 3
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 3
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 3
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 3