Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9997745
ACSL1
0.925 0.040 4 184816689 intron variant G/A snv 0.25 2
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs997509
ENPP1
0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs9957684 1.000 0.040 18 75154908 intergenic variant C/T snv 6.9E-02 2
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs9903658
ASIC2
1.000 0.040 17 33729207 intron variant A/G snv 0.11 2
rs972902
RORB
1.000 0.040 9 74562732 intron variant A/G snv 0.41 1
rs965384857
LPL
0.827 0.160 8 19954234 missense variant G/A snv 4.0E-06 5
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9514089
SLC10A2
0.882 0.080 13 103058487 intron variant T/C snv 0.41 3
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 4
rs934945
PER2
0.827 0.200 2 238246412 missense variant C/T snv 0.21 0.15 10
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs928940
IL1RN
0.882 0.120 2 113119918 intron variant G/T snv 0.78 3
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs926198
CAV1
0.851 0.120 7 116527154 intron variant C/A;T snv 4
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs916829
ABCC8
1.000 0.040 11 17418926 intron variant A/G;T snv 1
rs915654
LTA ; LOC100287329
1.000 0.040 6 31570720 upstream gene variant T/A;C snv 0.40 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs892051
ZNF98 ; LOC105376917
1.000 0.040 19 22506585 intron variant T/C snv 0.78 2