Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 2
rs11259936
ADAMTSL3
15 83911830 intron variant A/C;T snv 1
rs12338076
QSOX2
9 136229894 intron variant A/C;T snv 1
rs4932217 15 89358801 upstream gene variant A/C;T snv 0.54 1
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 4
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 3
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 3
rs3748069
ADGRG6
6 142446496 downstream gene variant A/G snv 0.39 3
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 2
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 2
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 2
rs2261033
PRRC2A
0.925 0.160 6 31635814 non coding transcript exon variant A/G snv 0.42 2
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 2
rs10187066
ZNF142
2 218650036 intron variant A/G snv 0.45 1
rs10401193
GATAD2A
19 19480257 intron variant A/G snv 0.19 1
rs1043515
PIP4K2B
17 38765943 3 prime UTR variant A/G snv 0.46 1
rs1046943
MICAL1 ; ZBTB24
1.000 0.040 6 109462738 3 prime UTR variant A/G snv 0.52 1
rs10519170 15 48393978 regulatory region variant A/G snv 0.18 1
rs10935120
CEP63
3 134514250 intron variant A/G snv 0.63 1
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56 1
rs110419
LOC105376536 ; LMO1
0.827 0.200 11 8231306 intron variant A/G snv 0.42 1
rs11082671
ZBTB7C
18 48339226 intron variant A/G snv 0.56 1
rs11648796
CIAO3
16 742190 upstream gene variant A/G snv 0.37 1
rs11830103
SBNO1
12 123338999 intron variant A/G snv 0.28 1
rs12075079
DNM3
1 172250855 intron variant A/G snv 0.16 1