Disease: Diabetes
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33