Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7