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: rs4132748
rs4132748
3 67405379 intron variant T/C snv 0.73
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs4674407
rs4674407
2 219517978 intron variant C/T snv 0.46
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs4721442
rs4721442
7 15466382 intron variant T/G snv 0.20
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs4809221
rs4809221
20 63741353 non coding transcript exon variant G/A;C;T snv 0.69; 3.2E-05
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs4885681
rs4885681
13 79893100 intron variant C/G;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs4952564
rs4952564
2 42016710 intron variant A/G snv 0.43
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs513953
rs513953
18 8801353 intron variant A/G;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs55884799
rs55884799
2 18106357 intron variant T/C snv 0.23
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs56196860
rs56196860
12 2799164 missense variant C/A snv 1.8E-02 2.0E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs59606152
rs59606152
17 81995068 synonymous variant C/G;T snv 7.2E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs62070648
rs62070648
17 30883577 intron variant G/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs6501431
rs6501431
17 70980274 intergenic variant C/T snv 0.81
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2014 2019
dbSNP: rs7041139
rs7041139
9 18013735 intron variant C/T snv 0.37
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs72902177
rs72902177
2 156159745 intron variant C/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs76219171
rs76219171
16 50155018 intron variant G/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs7838717
rs7838717
1.000 0.120 8 144280310 intron variant C/T snv 0.30
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs7977418
rs7977418
12 28435309 intron variant T/C snv 0.40
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs803765
rs803765
13 71073456 intron variant C/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs8069451
rs8069451
17 39348680 intron variant T/C snv 0.39
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs878471
rs878471
1 150575271 3 prime UTR variant G/A snv 0.48
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs91731
rs91731
5 33334206 intergenic variant C/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2017 2019
dbSNP: rs9357446
rs9357446
6 44479861 intergenic variant G/A snv 0.64
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs9689096
rs9689096
6 34221115 downstream gene variant A/C snv 0.11
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs9788269
rs9788269
12 93801114 intron variant A/G snv 0.23
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 2 2019 2019
dbSNP: rs10005540
rs10005540
4 173660916 downstream gene variant C/G;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019