Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 1
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 1
rs1558861 11 116736721 regulatory region variant C/G;T snv 3
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 1
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
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 1
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs2259820
HNF1A
0.882 0.160 12 120997539 synonymous variant C/T snv 0.34 0.26 1
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 2
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 3
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 1