Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10049010 3 165771709 intron variant T/C snv 8.1E-02 1
rs10049434 3 165771245 intron variant G/C snv 8.1E-02 1
rs10049436 1.000 0.080 3 165771478 intron variant C/T snv 8.1E-02 2
rs1007845 3 165722308 intron variant C/A;G;T snv 1
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 5
rs10211196
CYP20A1
2 203265173 intron variant G/A snv 0.40 1
rs1036584 3 165897353 regulatory region variant C/G snv 0.14 1
rs1036585 3 165906046 intergenic variant A/G snv 0.15 1
rs10439267
NBEAL1
2 203058724 intron variant C/T snv 0.40 1
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs1047964
BACE1 ; RNF214
11 117286177 3 prime UTR variant G/A;C;T snv 1
rs10497870
NBEAL1
2 203105560 intron variant A/C;G snv 1
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs10513616 3 165749249 intron variant A/G snv 9.6E-02 1
rs10513619 3 165697049 intron variant G/A snv 8.4E-02 1
rs10513621 3 166009331 intergenic variant T/G snv 9.1E-02 1
rs10513622 3 166009461 intergenic variant G/A;C snv 1
rs10800805
LOC112268254 ; RNPEP
1 201990610 intron variant G/A;C snv 1
rs10936458 3 165867467 intergenic variant C/T snv 0.52 1
rs10936468 3 166041120 intergenic variant A/G snv 0.40 1
rs10936474 3 166207739 intergenic variant G/T snv 0.58 1
rs1096215 3 165971863 intergenic variant T/C snv 0.56 1
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5