Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 6
rs283813
NECTIN2
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16 6
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs12721109
APOC4 ; APOC4-APOC2
1.000 0.080 19 44943964 intron variant G/A snv 1.3E-02 4
rs387976
NECTIN2
1.000 0.080 19 44875803 intron variant A/C;T snv 4
rs4803763
NECTIN2
1.000 0.080 19 44854034 intron variant G/A;C snv 4
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 4
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 4
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9268877
HLA-DRB9
0.827 0.200 6 32463370 intron variant A/G;T snv 4
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 3
rs17646665
SORT1
1.000 0.080 1 109369429 intron variant A/G snv 5.8E-02 3
rs1885119
TRPC4AP
1.000 0.080 20 35057846 intron variant T/C snv 0.58 3
rs2065108
MMP24-AS1-EDEM2 ; EDEM2
1.000 0.080 20 35119019 intron variant C/T snv 0.61 3
rs285
LPL
1.000 0.080 8 19957678 intron variant C/T snv 0.59 3
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 3
rs6087664
TRPC4AP
1.000 0.080 20 35038413 intron variant C/A;G;T snv 3
rs6088692
TRPC4AP
1.000 0.080 20 35050785 intron variant A/G snv 0.58 3