Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 3
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 2
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 1
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 1
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 3
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 1
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 3
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 2
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 1
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20