Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 9
rs2567241
CLGN
4 140402008 missense variant C/A snv 5.2E-02 6.0E-02 4
rs784257
LOC105372130
1.000 0.080 18 55729968 intron variant T/A;C snv 4
rs838133
FGF21 ; FUT1
19 48756272 synonymous variant A/G;T snv 0.67; 4.0E-06 3
rs7924036
JMJD1C
10 63431885 intron variant G/A;T snv 3
rs7072776
MLLT10 ; LOC107984214
0.925 0.080 10 21744013 downstream gene variant A/G snv 0.65 3
rs33951980
MLXIPL
7 73615107 intron variant C/T snv 0.10 3
rs7619139
RARB
3 25068924 intron variant T/A snv 0.54 3
rs34562254
TNFRSF13B
1.000 0.160 17 16939677 missense variant G/A snv 0.14 0.12 3
rs11104632 12 87829908 intergenic variant G/A snv 0.16 2
rs8022678 14 98900353 intergenic variant A/C;G snv 2
rs35397826
ARSG ; SLC16A6
17 68273941 missense variant A/G snv 0.12 0.11 2
rs113918189
CEP83
12 94325241 intron variant C/T snv 6.9E-02 2
rs2984348
CITED1 ; LOC105373250
X 72308510 intron variant C/T snv 0.31 2
rs148173957
LOC105378976
1.000 0.040 5 56078195 intron variant TT/- del 8.2E-02 2
rs40465
LOC105379109
1.000 0.040 5 104646025 intron variant T/G snv 0.24 2
rs7113624
LOC107984361
11 87508051 regulatory region variant G/A;C snv 2
rs643428
SSBP3
1 54263185 intron variant C/G;T snv 2
rs7334078
STK24
13 98468230 intron variant T/C snv 0.29 2
rs13211840
UST
6 148791054 intron variant T/C snv 0.15 2