Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs2492301
LINC01137 ; ZC3H12A
1 37473572 intron variant T/C snv 0.53 4
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 3
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77 3
rs10751450
ATP2B4
1 203681817 intron variant C/G;T snv 2
rs10923397 1 117708521 regulatory region variant C/T snv 0.14 2
rs12563213 1 154318779 upstream gene variant G/C snv 0.30 2
rs148046772
CCT3
1 156314104 intron variant A/C;T snv 2
rs1578741 1 117716081 intergenic variant A/C snv 0.19 2
rs34544423 1 198578103 regulatory region variant C/G snv 6.4E-02 2
rs35229050
E2F2
1 23514124 intron variant AA/-;A;AAA delins 0.53 2
rs35340377
TRIM58
1 247874908 intron variant G/A snv 0.23 2
rs3962382 1 67700010 downstream gene variant A/C;G snv 2
rs6540555
TRAF3IP3
1 209763226 intron variant A/G snv 0.36 2
rs826415
TENT5C
1 117611355 intron variant T/G snv 0.27 2
rs11204538 1 247882970 downstream gene variant C/T snv 0.55 1
rs112521149
CLCN6
1 11829758 intron variant G/A snv 6.0E-02 1
rs11464707
TENT5C
1 117618398 intron variant T/G snv 0.18 1
rs11581122
TENT5C
1 117626204 3 prime UTR variant C/T snv 0.14 1
rs12083184
OR10Z1
1 158609130 3 prime UTR variant G/C;T snv 1