Disease: elevated blood glucose level
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 17
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 16
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16