Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11573213
PLA2G5
1 20075517 intron variant A/C;G snv 1
rs11760826
LOC105375434 ; NAPEPLD
7 103151364 upstream gene variant A/C;G snv 1
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs325465
NPSR1-AS1 ; NPSR1
7 34811812 missense variant A/C;G;T snv 4.0E-06; 2.3E-03 1
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 1
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs485671
LIPC ; ALDH1A2 ; LIPC-AS1
15 58448935 intron variant A/C;T snv 5
rs387976
NECTIN2
1.000 0.080 19 44875803 intron variant A/C;T snv 4
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 3
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 3
rs970548
MARCHF8
10 45517829 intron variant A/C;T snv 3
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
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7