Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5