Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11383346
LOC107984462 ; LOC105369710
12 28130254 upstream gene variant -/T delins 0.58 2
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs1102077 6 139950220 intron variant A/C snv 0.21 3
rs1595029
RSRC1
3 158523978 intron variant A/C snv 0.52 2
rs17009288 1 221030957 regulatory region variant A/C snv 0.30 2
rs2202572
LINC01416
18 55899240 intron variant A/C snv 0.66 2
rs9689096 6 34221115 downstream gene variant A/C snv 0.11 2
rs10410606
LTBP4
19 40603069 intron variant A/C snv 0.52 1
rs1248079
GRK5
10 119361783 intron variant A/C snv 0.11 1
rs17533219 18 56380190 regulatory region variant A/C snv 0.32 1
rs17631425 2 104896266 intron variant A/C snv 0.68 1
rs2863171
PRDM11
11 45229181 3 prime UTR variant A/C snv 0.21 1
rs34003290
RAD18
3 8887207 intron variant A/C snv 0.17 1
rs35399441
PLAG1
8 56176872 intron variant A/C snv 0.26 1
rs4693978
FAM13A ; LOC105377327
4 88933016 intron variant A/C snv 0.56 1
rs6061555
GATA5
20 62474494 intron variant A/C snv 0.63 1
rs62127635 2 52501410 upstream gene variant A/C snv 0.24 1
rs6657854
LOC105372932
1 221457213 regulatory region variant A/C snv 0.22 1
rs669052
FEZ1
11 125472234 intron variant A/C snv 9.9E-02 1
rs67513858
RHBDD1
2 226940103 intron variant A/C snv 0.46 1
rs7108992
ETS1
11 128511972 intron variant A/C snv 0.71 1
rs74453786
EIF4E2
2 232576992 intron variant A/C snv 3.9E-02 1
rs759869 7 24103309 intergenic variant A/C snv 0.74 1
rs7614311
C3orf49
3 63827978 intron variant A/C snv 0.15 1
rs9401305 6 97884061 intron variant A/C snv 0.41 1