Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10500212
PBX4
19 19612406 intron variant C/T snv 0.10 4
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 2
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 2
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 5
rs1077514
ASAP3
1 23439740 intron variant C/T snv 0.75 1
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
rs10788994 1 55035303 upstream gene variant C/T snv 0.20 3
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs10858082
CELSR2
1 109256099 intron variant G/A snv 0.48 3
rs10888898
PCSK9
1 55050835 intron variant A/G snv 0.59 3
rs10889333
DOCK7
1 62491359 intron variant G/A snv 0.33 1
rs10889338
DOCK7
1 62519226 intron variant C/T snv 0.34 2
rs10889348
DOCK7
1 62612551 intron variant A/T snv 0.32 1
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 3
rs10903129
MACO1
1 25442446 intron variant A/G snv 0.58 2
rs10904908
VIM-AS1
10 17218291 intron variant A/G snv 0.41 1
rs10916704
PLA2G5
1 20074498 intron variant G/A;T snv 3
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs11076174
CETP
16 56969234 intron variant T/C snv 0.10 2
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 4
rs11102967
CELSR2
1 109274623 3 prime UTR variant C/G;T snv 0.55 1