Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10850377
rs10850377
12 114763631 intron variant G/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 3 2015 2019
dbSNP: rs2637254
rs2637254
10 76552244 intron variant G/A snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 3 2017 2019
dbSNP: rs10141786
rs10141786
14 74350715 intron variant A/G snv 0.67
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs10498672
rs10498672
6 7797607 intron variant C/G snv 0.13
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs10998018
rs10998018
10 68203197 intron variant G/A snv 0.41
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs11176001
rs11176001
12 66015587 regulatory region variant C/A snv 9.6E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs11191841
rs11191841
10 103879853 3 prime UTR variant T/C snv 0.47
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs11621587
rs11621587
14 92631994 intron variant G/C;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs1192415
rs1192415
0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs12497779
rs12497779
3 99103206 intergenic variant G/T snv 0.25
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs12634907
rs12634907
3 158509097 intron variant A/G snv 0.28
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs12698403
rs12698403
7 156334552 intergenic variant G/A snv 0.40
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs143384
rs143384
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs1513272
rs1513272
7 28160478 intron variant C/T snv 0.40
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs17009288
rs17009288
1 221030957 regulatory region variant A/C snv 0.30
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs2076295
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs2345443
rs2345443
16 78191736 intron variant A/C;G snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs2441026
rs2441026
5 54148668 intron variant C/T snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2017 2019
dbSNP: rs2571445
rs2571445
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2017 2019
dbSNP: rs2812208
rs2812208
13 50132951 intron variant G/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs34712979
rs34712979
1.000 0.040 4 105897896 splice region variant G/A;T snv 0.17
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2017 2019
dbSNP: rs35043843
rs35043843
1 118368672 intergenic variant T/G snv 0.21
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs35506
rs35506
12 115062886 intergenic variant T/A snv 0.76
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2017 2019
dbSNP: rs3751837
rs3751837
16 3533173 3 prime UTR variant C/A;T snv 0.22 0.23
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs3791679
rs3791679
0.925 0.120 2 55869757 intron variant A/G snv 0.20
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019