Disease: Forced expiratory volume function
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
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
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
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 5
rs55958997
CHRNB4
1.000 0.040 15 78623530 upstream gene variant C/A snv 0.32 5
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs12902602
LOC112268142 ; CHRNB4
15 78675059 intron variant A/G snv 0.28 4
rs2316205 19 40840863 non coding transcript exon variant T/C snv 0.40 4
rs113029345 19 40864271 intron variant T/C snv 3
rs34684276
HYKK
15 78520813 intron variant G/A snv 0.24 3
rs667282
CHRNA5
0.790 0.120 15 78571130 intron variant T/C snv 0.28 3
rs8079868
MYHAS
17 10617383 intron variant T/C snv 0.22 2