Disease: Forced expiratory volume function
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 8
rs55781567
CHRNA5
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31 7
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs138544659
CHRNA3
1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs190065944
CHRNA5
0.925 0.080 15 78567268 intron variant G/A snv 3.4E-03 5
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 5
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs34712979
NPNT
1.000 0.040 4 105897896 splice region variant G/A;T snv 0.17 5
rs55958997
CHRNB4
1.000 0.040 15 78623530 upstream gene variant C/A snv 0.32 5
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 5
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 4
rs12504628
LOC105377462
1.000 0.040 4 144515172 intron variant T/C snv 0.33 4
rs1529672
RARB
1.000 0.040 3 25479091 intron variant C/A;T snv 4
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 4
rs2955083
EEFSEC
1.000 0.040 3 128242335 intron variant T/A snv 0.89 4
rs4243084
CHRNA3
1.000 0.040 15 78619330 intron variant G/C snv 0.30 4
rs4416442
LOC105377327 ; FAM13A
0.925 0.080 4 88945562 intron variant T/C snv 0.45 4
rs55853698
CHRNA5
0.882 0.080 15 78565597 5 prime UTR variant T/G snv 0.25 4
rs8031948
HYKK
1.000 0.040 15 78523715 intron variant G/T snv 0.27 4
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 4