Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
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
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 3
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 2
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs767455
TNFRSF1A
0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 1