Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2908289
GCK ; LOC105375257
1.000 0.080 7 44184343 intron variant G/A snv 0.20 3
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs343
LPL
1.000 0.080 8 19953276 intron variant C/A snv 9.8E-02 8.1E-02 3
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs4458523
WFS1
1.000 0.080 4 6288259 intron variant T/G snv 0.61 3
rs4502156 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 3
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 3
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 3
rs7025162 1.000 0.080 9 133290774 regulatory region variant T/C snv 0.82 3
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 3
rs7708285
ZBED3-AS1
1.000 0.080 5 77130042 intron variant G/A snv 0.76 3
rs7766070
CDKAL1
1.000 0.080 6 20686342 intron variant C/A snv 0.25 3
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 3
rs9368219
CDKAL1
1.000 0.080 6 20674460 intron variant C/T snv 0.19 3
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 2
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 2
rs1183910
HNF1A
1.000 0.080 12 120983004 intron variant G/A snv 0.28 2
rs12427353
HNF1A
1.000 0.080 12 120989098 intron variant G/A;C;T snv 2
rs174450
FADS3
1.000 0.080 11 61874070 intron variant G/T snv 0.44 2
rs174602
FADS2
1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 2
rs174616
FADS2
1.000 0.080 11 61861650 intron variant G/A snv 0.51 2
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 2
rs2250417
BCO2
1.000 0.080 11 112214593 intron variant T/C snv 0.44 2
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs2497304 1.000 0.080 10 92732959 intergenic variant C/T snv 0.36 2