Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs7016880 8 20019235 intergenic variant G/C snv 8.5E-02 2
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 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
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 2
rs3812316
MLXIPL
0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 2
rs11206517
PCSK9
1.000 0.120 1 55060755 intron variant T/C;G snv 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
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
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 1
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 1
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 1
rs2259820
HNF1A
0.882 0.160 12 120997539 synonymous variant C/T snv 0.34 0.26 1
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 1
rs972283
LOC105375508
1.000 0.080 7 130782095 intergenic variant A/G;T snv 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1