Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 7
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 7
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs724016
ZBTB38
1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52 5
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 4
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13 4