Disease: Vital capacity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 9
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs11722225
INTS12 ; GSTCD
4 105845273 intron variant T/C snv 5.5E-02 5
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
rs117068593
RIN3
14 92651884 missense variant C/T snv 0.13 0.11 4
rs12198986 6 7719826 regulatory region variant G/A snv 0.37 4
rs13116999
LOC105377462
4 144521212 intron variant G/A snv 0.65 4
rs1496255 4 120683279 downstream gene variant G/A;T snv 4
rs1513272
JAZF1
7 28160478 intron variant C/T snv 0.40 4
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39 4
rs6780171
IGF2BP2
3 185785668 intron variant T/A snv 0.39 4
rs6918725
LOC105377992
6 126669246 intron variant T/G snv 0.50 4
rs7155279
TRIP11
14 92019537 intron variant G/A;T snv 4
rs7424771
RBMS1
2 160419867 intron variant G/A snv 0.44 4
rs7752448
ZSCAN31
6 28333322 intron variant A/G snv 0.15 4
rs8042849
HYKK
1.000 0.040 15 78525587 intron variant C/T snv 0.65 4
rs916888
LRRC37A2 ; WNT3
17 46785767 intron variant T/C snv 0.19 4
rs1008833
PIK3C2B
1 204457167 intron variant A/G snv 0.12 3
rs10998018
MYPN
10 68203197 intron variant G/A snv 0.41 3