Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs2292596
AHRR
0.827 0.240 5 422840 missense variant C/G;T snv 0.38; 4.0E-06 7
rs3134945
RNF5 ; MIR6833 ; AGPAT1
0.827 0.240 6 32178715 intron variant C/A snv 0.18 6
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 5
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs3217992
CDKN2B-AS1 ; CDKN2B
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs35829419
NLRP3
0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34