Source: INFERRED ×
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 23
rs113993959
CFTR
0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 19
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs74597325
CFTR
0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 13
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 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
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 8
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 8
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 8
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 8
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 8
rs17580
SERPINA1
0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 8
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 7
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 7
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 7
rs55781567
CHRNA5
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31 7
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7