Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 2
rs74380195 1.000 0.080 11 103016500 intergenic variant A/G snv 0.11 1
rs7921536
SH3PXD2A
1.000 0.080 10 103597080 3 prime UTR variant A/G snv 3.5E-02 1
rs12248541
SH3PXD2A
1.000 0.080 10 103630585 intron variant A/G snv 4.2E-02 1
rs325485
LOC105379109
0.925 0.120 5 104659667 intron variant A/G snv 0.65 2
rs396755
LOC105379109
0.925 0.120 5 104686538 intron variant C/G snv 0.61 2
rs662064
PEX14
1.000 0.080 1 10497194 intron variant T/C snv 0.66 1
rs7733624 1.000 0.080 5 105131414 intron variant C/A;T snv 1
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs6967330
CDHR3
0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 1
rs6959584
CDHR3
1.000 0.080 7 106036059 3 prime UTR variant C/T snv 0.12 1
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs7936275
MRVI1
1.000 0.080 11 10639293 intron variant G/T snv 0.24 1
rs2052690
MRVI1
0.925 0.080 11 10642486 intron variant G/T snv 0.22 2
rs793607
DUBR
1.000 0.080 3 107340876 intron variant G/A;C snv 2
rs7521681
VAV3
0.925 0.120 1 107779913 intron variant G/A snv 0.15 2
rs4957798
FER
1.000 0.080 5 109108853 intron variant C/T snv 0.19 1
rs114356520 1.000 0.080 9 109366718 intergenic variant G/A;C snv 1
rs6982751
XKR6
0.925 0.120 8 10955964 intron variant C/G;T snv 2
rs7705653 1.000 0.080 5 110807116 regulatory region variant A/G snv 0.29 2
rs17513503 0.882 0.120 5 110810746 intergenic variant C/A;G snv 2
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 3
rs7734635 0.925 0.080 5 110823145 intergenic variant A/G snv 0.30 3
rs540485182 0.925 0.080 5 110825774 intergenic variant -/A;AA;AAA delins 2