Disease: elevated blood glucose level
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
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
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 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
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16