Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs1558861 11 116736721 regulatory region variant C/G;T snv 3
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 3
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs7016880 8 20019235 intergenic variant G/C snv 8.5E-02 2
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs4635554 2 21166787 intergenic variant T/G snv 0.37 1
rs9644568 8 20071071 intergenic variant G/A snv 0.11 1
rs9949617
TMEM241
18 23299253 intron variant C/T snv 0.22 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
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
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 2