Disease: Respiratory Function Tests
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
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 7
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 5
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 5
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs12504628
LOC105377462
1.000 0.040 4 144515172 intron variant T/C snv 0.33 4
rs1496255 4 120683279 downstream gene variant G/A;T snv 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
rs8031948
HYKK
1.000 0.040 15 78523715 intron variant G/T snv 0.27 4
rs13147758
LOC105377462
4 144539078 intron variant A/G snv 0.31 3
rs1541374 4 105127203 intergenic variant T/A;G snv 3
rs1980057 1.000 0.040 4 144564586 intron variant C/T snv 0.31 3
rs2798641
ARMC2
6 108946847 intron variant C/T snv 0.15 3
rs347412
DGKH
1.000 0.080 13 42212544 intron variant A/G;T snv 3
rs7068966
CDC123
1.000 0.040 10 12235993 intron variant C/T snv 0.43 3
rs8089099 18 10078074 regulatory region variant G/A snv 0.22 3
rs10516526
GSTCD ; GSTCD-AS1 ; INTS12
4 105767747 intron variant A/G snv 5.4E-02 2
rs11001819
LRMDA
10 76555466 intron variant G/A snv 0.41 2
rs11654749
CASC17
17 71129465 intron variant G/T snv 0.30 2
rs11727189
INTS12 ; ARHGEF38
4 105697983 intron variant G/T snv 5.4E-02 2
rs12477314 2 238955452 regulatory region variant C/G;T snv 2