Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs10422058
ARMC6
19 19047391 intron variant T/A;C snv 2
rs10427943
CABIN1
22 24131331 intron variant G/T snv 1.2E-02 2
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02 4
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 2
rs10501321
MADD-AS1 ; MADD
11 47273075 intron variant T/C snv 0.42 2
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs1059507
LPL
1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 3
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 2
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 5
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 2
rs10773105
SCARB1
12 124799220 intron variant C/T snv 0.63 2
rs10773112
SCARB1
12 124853983 intron variant C/T snv 0.63 2
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 1
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs10792832 1.000 0.080 11 86156833 downstream gene variant A/G snv 0.70 1
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs10818782
GABBR2
9 98325004 intron variant G/A snv 0.60 2
rs10838681
NR1H3
1.000 0.040 11 47253513 intron variant G/A snv 0.34 1