Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 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
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02 5
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 5
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs12708967 16 56959299 upstream gene variant T/C snv 0.18 4
rs17411126 8 19997761 intergenic variant T/C snv 0.26 4
rs17489268 8 19994534 regulatory region variant T/A snv 0.25 4
rs327
LPL
8 19962025 intron variant T/G snv 0.31 4
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs17091905 8 19992246 intergenic variant G/A snv 0.17 2
rs3213545
OASL
12 121033534 synonymous variant G/A snv 0.32 0.26 2
rs10049010 3 165771709 intron variant T/C snv 8.1E-02 1
rs10049434 3 165771245 intron variant G/C snv 8.1E-02 1
rs1007845 3 165722308 intron variant C/A;G;T snv 1
rs10211196
CYP20A1
2 203265173 intron variant G/A snv 0.40 1