Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801262
NEUROD1 ; CERKL
0.882 0.120 2 181678728 missense variant T/C snv 0.70 0.68 4
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs2281068
APLN
0.925 0.080 X 129653796 intron variant T/C snv 0.31 3
rs2281939
SORBS1
0.790 0.320 10 95414595 missense variant T/C snv 8.2E-02 0.13 9
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2779248
NOS2
0.882 0.160 17 27800806 intron variant T/C snv 0.39 4
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3767434
POU2F1
0.925 0.080 1 167401914 intron variant T/C snv 0.14 3
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs4917
AHSG
0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 9
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs6902123
PPARD
0.925 0.080 6 35362644 intron variant T/C snv 0.24 3
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs7204609
FTO
0.827 0.200 16 53799693 intron variant T/C snv 0.14 6
rs735949
ACSL1
0.925 0.080 4 184795078 intron variant T/C snv 0.10 3
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs7578597
THADA
0.807 0.240 2 43505684 missense variant T/C snv 9.9E-02 0.14 7
rs769985775
DMD
0.851 0.160 X 32448630 synonymous variant T/C snv 5.7E-06 9.5E-06 6
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8065080
TRPV1
0.827 0.200 17 3577153 missense variant T/C snv 0.37 0.32 11