Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs75686861
HHIP
0.790 0.080 4 144700176 intron variant G/A snv 6.3E-02 10
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 8
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs2294214
CASC15
0.882 0.040 6 22056694 splice region variant A/C;T snv 6
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs34712979
NPNT
1.000 0.040 4 105897896 splice region variant G/A;T snv 0.17 5
rs1496255 4 120683279 downstream gene variant G/A;T snv 4
rs442177
AFF1
4 87109109 intron variant G/T snv 0.56 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 4
rs8042849
HYKK
1.000 0.040 15 78525587 intron variant C/T snv 0.65 4
rs6780171
IGF2BP2
3 185785668 intron variant T/A snv 0.39 4
rs1513272
JAZF1
7 28160478 intron variant C/T snv 0.40 4
rs13116999
LOC105377462
4 144521212 intron variant G/A snv 0.65 4
rs6918725
LOC105377992
6 126669246 intron variant T/G snv 0.50 4
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39 4