Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 3
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 3
rs17110429
PPARGC1B
5 149800331 intron variant A/C snv 3.5E-02 2
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 2
rs1826361
AGTR1
3 148726941 intron variant A/C snv 0.13 2
rs2819371
LMOD1
1 201946530 5 prime UTR variant A/C snv 0.92 2
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 1
rs12113155
PRKAG2
7 151607887 intron variant A/C;G snv 3
rs13465
ILF3
19 10692116 3 prime UTR variant A/C;G snv 3
rs598962
ABCD3
1 94451093 intron variant A/C;G snv 3
rs655246 1 109289661 downstream gene variant A/C;G snv 3
rs7162932
TPM1
15 63060452 intron variant A/C;G snv 3
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 2
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 2
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2328223 20 17865277 intergenic variant A/C;G;T snv 2
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
rs12394306
SYN1
X 47576648 splice region variant A/C;T snv 4.3E-03 4
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
rs486438
PDE4B
1 66208980 intron variant A/C;T snv 2