Disease: Forced expiratory volume function
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 18
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 11
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 9
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 9
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs13118928 0.925 0.040 4 144565237 intron variant A/G snv 0.33 7
rs1489759
LOC105377462
0.882 0.080 4 144553321 intron variant A/G snv 0.43 7
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 7
rs7671167
FAM13A
0.925 0.040 4 88962828 intron variant C/T snv 0.53 7
rs12504628
LOC105377462
1.000 0.040 4 144515172 intron variant T/C snv 0.33 6
rs1529672
RARB
1.000 0.040 3 25479091 intron variant C/A;T snv 6
rs1980057 1.000 0.040 4 144564586 intron variant C/T snv 0.31 6
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 6
rs11722225
INTS12 ; GSTCD
4 105845273 intron variant T/C snv 5.5E-02 5
rs13147758
LOC105377462
4 144539078 intron variant A/G snv 0.31 5
rs1512282
LOC105377462
4 144510345 intron variant A/C;G snv 0.33 5
rs1512288 1.000 0.040 4 144570129 intron variant G/A snv 0.42 5
rs1541374 4 105127203 intergenic variant T/A;G snv 5
rs1828591
LOC105377462
1.000 0.040 4 144559628 intron variant A/G snv 0.43 5
rs2013701
FAM13A
1.000 0.040 4 88963935 intron variant G/T snv 0.51 5
rs2045517
LOC105377327 ; FAM13A
4 88949813 intron variant C/T snv 0.49 5