Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 8
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 7
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 7
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs4757268
PDE3B
0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28 5
rs2267443
SREBF2
0.882 0.120 22 41891450 intron variant A/G snv 0.67 5
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5
rs6494005
ALDH1A2 ; LIPC
1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 5
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 4
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs1051295
KCNB1 ; LOC105372649
0.925 0.080 20 49372368 3 prime UTR variant A/G snv 0.22 3
rs1052717
SREBF2
0.925 0.080 22 41885425 intron variant A/G snv 0.62 3
rs11569562
C3
0.882 0.160 19 6678742 intron variant A/G snv 0.50 3
rs13226650
MLXIPL
1.000 0.040 7 73602675 intron variant A/G snv 0.19 3
rs2845573
FADS2
1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 3
rs5742912
SCNN1A ; LOC107984500
0.925 0.160 12 6349184 missense variant A/G snv 1.9E-02 1.7E-02 3
rs6993
GOT2
0.925 0.080 16 58707463 3 prime UTR variant A/G snv 0.59 3
rs10247649
PDK4
0.925 0.080 7 95586935 non coding transcript exon variant A/G snv 0.43 2
rs10484092
FRMD6-AS2 ; FRMD6
1.000 0.040 14 51489516 intron variant A/G snv 4.8E-02 2