Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3731215
CDKN2A
9 21985772 intron variant A/G snv 1.2E-03 5
rs4253440
CEBPB-AS1 ; CEBPB
20 50191616 missense variant G/A snv 1.4E-03 5
rs4253642
LOC105373074 ; PPARA
22 46167520 intron variant A/G snv 7.1E-03 5
rs473224
LIPC-AS1 ; ALDH1A2 ; LIPC
15 58445142 intron variant T/A;G snv 5
rs485538
LIPC ; ALDH1A2 ; LIPC-AS1
15 58448978 intron variant C/G;T snv 5
rs485671
LIPC ; ALDH1A2 ; LIPC-AS1
15 58448935 intron variant A/C;T snv 5
rs4938303 11 116714271 intergenic variant C/A;T snv 0.62 5
rs5030339
LOC105372272 ; ICAM1
19 10269461 intron variant G/A snv 3.4E-03 5
rs588136
ALDH1A2 ; LIPC ; LIPC-AS1
15 58438299 intron variant C/G;T snv 5
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs7000184
BAG4 ; LSM1
8 38176676 5 prime UTR variant C/T snv 2.3E-02 5
rs7666097
KDR
4 55124971 intron variant T/A;C snv 5
rs8033940
ALDH1A2 ; LIPC
15 58432643 intron variant G/A snv 0.41 5
rs8034802
ALDH1A2 ; LIPC
15 58432593 intron variant T/A snv 0.33 5
rs8039217
STARD9
15 42694939 intron variant C/A snv 4.1E-02 5
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs9436735
LEPR ; LEPROT
1 65419378 upstream gene variant C/G snv 2.5E-02 5
rs9658292
NOS1
12 117318980 intron variant G/C snv 9.4E-04 5
rs10107815
MSRA
8 10156645 intron variant G/C snv 5.1E-02 4
rs10271556
NAMPT
7 106258428 intron variant C/T snv 5.6E-02 4
rs10402729
NCAN
19 19244291 intron variant T/C snv 3.3E-02 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02 4