Disease: Vital capacity
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
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
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs2294214
CASC15
0.882 0.040 6 22056694 splice region variant A/C;T snv 6
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs6918725
LOC105377992
6 126669246 intron variant T/G snv 0.50 4
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs117642368 17 45321692 upstream gene variant G/C snv 6.9E-02 3
rs12198986 6 7719826 regulatory region variant G/A snv 0.37 3
rs34093919
LTBP4
19 40611394 missense variant G/A snv 7.7E-03 7.5E-03 3
rs4252548
IL11
1.000 0.040 19 55368304 missense variant C/T snv 2.1E-02 1.8E-02 3
rs7155279
TRIP11
14 92019537 intron variant G/A;T snv 3
rs8067165
LOC105376799
17 8128618 upstream gene variant C/A;G;T snv 3
rs9435733
MFAP2
1 16981759 intron variant T/C snv 0.41 3
rs1000972 20 6641070 regulatory region variant T/A;G snv 2
rs1074765 6 109360458 intergenic variant T/C snv 0.52 2
rs1388242 6 45682278 TF binding site variant T/C snv 0.35 2
rs1472565
CAPZB
1 19428536 intron variant T/A;C snv 2
rs17134767
GMDS
6 2195682 intron variant T/C snv 0.31 2
rs187799739
RPRD2
1 150452900 intron variant C/A;G snv 2
rs2079795 17 61419288 regulatory region variant T/A;C snv 2
rs2179687
SLX4IP
20 10633647 intron variant A/G snv 0.72 2
rs4337252
LOXL1
1.000 0.040 15 73934424 intron variant G/C snv 0.52 2