Disease: Diabetes
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4
rs113296370
PLEKHH2
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 5
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs11124945
PLEKHH2
1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1269801977
PPIG
0.925 0.120 2 169604087 missense variant A/G snv 4.0E-06 7.0E-06 4
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 7
rs2276047
INPPL1
1.000 0.040 11 72230337 intron variant A/G snv 0.28 0.33 3
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9