Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 6
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6