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
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
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
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
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
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs9368649 0.925 0.040 6 30971106 intergenic variant A/G snv 0.10 7
rs1980057 1.000 0.040 4 144564586 intron variant C/T snv 0.31 6
rs12504628
LOC105377462
1.000 0.040 4 144515172 intron variant T/C snv 0.33 6
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 6
rs1529672
RARB
1.000 0.040 3 25479091 intron variant C/A;T snv 6
rs1541374 4 105127203 intergenic variant T/A;G snv 5
rs2798641
ARMC2
6 108946847 intron variant C/T snv 0.15 5
rs7068966
CDC123
1.000 0.040 10 12235993 intron variant C/T snv 0.43 5
rs2865531
CFDP1
1.000 0.040 16 75356418 intron variant T/A snv 0.52 5
rs7733088
HTR4 ; LOC107986462
1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 5
rs8031948
HYKK
1.000 0.040 15 78523715 intron variant G/T snv 0.27 5
rs13147758
LOC105377462
4 144539078 intron variant A/G snv 0.31 5
rs3995090
LOC107986462 ; HTR4
1.000 0.040 5 148466252 intron variant A/C snv 0.39 5
rs12477314 2 238955452 regulatory region variant C/G;T snv 4
rs1496255 4 120683279 downstream gene variant G/A;T snv 4