Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397948882 0.925 0.040 7 15597253 intergenic variant -/A delins 2.9E-04 2
rs10493390
PDE4B
0.925 0.040 1 65846910 intron variant A/C snv 1.7E-02 2
rs10748401
NELL2
0.925 0.040 12 44758763 intron variant A/C snv 0.71 2
rs10858818
LINC02458
0.925 0.040 12 89032955 intron variant A/C snv 0.21 2
rs11096128 0.925 0.040 X 144414767 intergenic variant A/C snv 9.6E-02 2
rs11177789
BEST3 ; LOC105369823
0.925 0.040 12 69679438 intron variant A/C snv 0.11 2
rs11921493
CMC1
0.925 0.040 3 28261297 intron variant A/C snv 4.8E-02 2
rs16846805 0.925 0.040 4 71659040 intergenic variant A/C snv 3.6E-02 2
rs16862035
NAALADL2
0.925 0.040 3 174577089 intron variant A/C snv 2.1E-02 2
rs17027607
TSPAN5
0.925 0.040 4 98470950 3 prime UTR variant A/C snv 0.11 2
rs17031683
LOC105369938 ; MYBPC1
0.925 0.040 12 101611608 intron variant A/C snv 6.0E-02 2
rs17618877
EXPH5
0.925 0.040 11 108509147 3 prime UTR variant A/C snv 8.7E-02 2
rs1905041
MSC-AS1
0.925 0.040 8 71837329 intron variant A/C snv 0.27 2
rs246478
LOC105378234
0.925 0.040 5 151355071 intergenic variant A/C snv 0.18 2
rs267689 0.925 0.040 1 29993005 intergenic variant A/C snv 8.5E-02 2
rs2831758
LOC105372764
0.925 0.040 21 28394475 intron variant A/C snv 0.15 2
rs2925763
ITGB6
0.925 0.040 2 160160265 intron variant A/C snv 0.19 2
rs3803070
PLXNC1 ; CEP83
0.925 0.040 12 94294912 intron variant A/C snv 0.21 2
rs4764080 0.925 0.040 12 14336617 intergenic variant A/C snv 0.54 2
rs4916753
LOC107986387
0.925 0.040 5 89491366 intergenic variant A/C snv 0.81 2
rs645078
RPS6KA4 ; MIR1237
0.925 0.040 11 64367826 intron variant A/C snv 0.29 2
rs6729895
PTH2R ; LOC101927960
0.925 0.040 2 208584803 intron variant A/C snv 0.16 2
rs7079515
ADK
0.925 0.040 10 74272653 intron variant A/C snv 4.7E-02 2
rs7175718
ADAMTSL3
0.882 0.120 15 83900350 intron variant A/C snv 1.6E-02 2
rs7648547 0.925 0.040 3 41146509 intergenic variant A/C snv 0.45 2