Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs760242
DHCR7
11 71435530 missense variant C/T snv 2.2E-04 6.3E-05 6
rs7993724
PDX1 ; PLUT
13 27919139 upstream gene variant T/C snv 5.6E-03 6
rs8138057
PDXP
22 37665537 intron variant G/A snv 3.0E-03 1.3E-02 6
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02 5
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs1456649
FMN2
1 240288305 intron variant G/C snv 3.0E-03 5
rs16880248
CNR1
6 88141968 3 prime UTR variant G/T snv 2.7E-02 5
rs17243641
LOC105376326 ; TRAF2 ; MIR4479
9 136886986 intron variant G/T snv 2.6E-03 5
rs17513478
RIPK1
6 3101321 intron variant G/A snv 5.7E-03 5
rs180327
BUD13
11 116752943 intron variant C/T snv 0.58 5
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs261336
ALDH1A2 ; LIPC ; LIPC-AS1
15 58450219 intron variant G/A snv 0.81 5
rs261338
LIPC ; LIPC-AS1 ; ALDH1A2
15 58442806 intron variant A/G snv 0.83 5
rs261342
LIPC-AS1 ; LIPC ; ALDH1A2
15 58438954 intron variant G/A;C;T snv 5
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
rs34660894
LRP1 ; STAT6
12 57129111 intron variant G/A snv 2.3E-03 1.0E-02 5
rs35738419
RXRA
9 134411944 intron variant C/T snv 7.3E-04 5