Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 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
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs1558861 11 116736721 regulatory region variant C/G;T snv 3
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs11206517
PCSK9
1.000 0.120 1 55060755 intron variant T/C;G snv 2
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 2
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 2
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 1
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs972283
LOC105375508
1.000 0.080 7 130782095 intergenic variant A/G;T snv 1
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 4
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs7016880 8 20019235 intergenic variant G/C snv 8.5E-02 2
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs3812316
MLXIPL
0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 2
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 6
rs9644568 8 20071071 intergenic variant G/A snv 0.11 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs9949617
TMEM241
18 23299253 intron variant C/T snv 0.22 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5