Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs1558861 11 116736721 regulatory region variant C/G;T snv 3
rs7016880 8 20019235 intergenic variant G/C snv 8.5E-02 2
rs11634397 1.000 0.080 15 80139880 downstream gene variant A/G snv 0.57 1
rs4635554 2 21166787 intergenic variant T/G snv 0.37 1
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 1
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 1
rs9644568 8 20071071 intergenic variant G/A snv 0.11 1
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 3
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 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
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 1
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 1
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 1