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
rs188344082 1.000 0.040 1 18783262 intergenic variant G/A snv 1.8E-02 3
rs61823501
C1orf21
1.000 0.040 1 184396836 intron variant C/T snv 0.12 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs74056623 1.000 0.040 1 18784584 intergenic variant G/A snv 8.3E-02 3
rs74056624 1.000 0.040 1 18790006 intergenic variant G/A snv 2.3E-02 3
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 2
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
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
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 2
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs189919070
MIR4788
1.000 0.040 3 134436825 upstream gene variant C/A;T snv 3
rs12638540
CMTM7
1.000 0.040 3 32447042 intron variant A/G;T snv 1
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
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 1
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18