Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397514580
GCK ; LOC105375258
0.925 0.080 7 44146467 missense variant C/T snv 2
rs534828104
AHSG
0.925 0.080 3 186618566 missense variant A/G snv 2
rs556581174
GCK
0.925 0.080 7 44145637 stop gained G/A;C;T snv 2
rs8066560
SREBF1
0.925 0.040 17 17824729 intron variant A/G snv 0.64 2
rs9906827
RPTOR
0.925 0.120 17 80691605 intron variant C/A;T snv 2
rs10139403
DLK1
1.000 0.040 14 100728224 intron variant A/G snv 0.62 1
rs1410713 1.000 0.040 20 3079704 downstream gene variant A/C snv 0.62 1
rs2282018
AVP
1.000 0.040 20 3084303 intron variant C/T snv 0.60 1
rs2770381 1.000 0.040 20 3081340 downstream gene variant A/C snv 0.35 1
rs6084264
AVP
1.000 0.040 20 3089925 upstream gene variant T/C snv 0.58 1
rs1447680989
GCKR
1.000 0.040 2 27501147 missense variant G/A snv 4.0E-06 1
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs746913146
LOC105375258 ; GCK
1.000 0.040 7 44149816 missense variant G/A snv 4.0E-06 1
rs764232985
GCK
0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 4
rs775776658
ABCC8
1.000 0.040 11 17474926 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.0E-05 1
rs193922289
GCK
0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 3
rs369841551
MC4R
0.882 0.120 18 60371884 stop gained G/A;T snv 4.0E-06 3
rs193922287
GCK
0.925 0.080 7 44153334 missense variant G/A snv 4.0E-06 2
rs587777042
CYC1
0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs751279776
LOC105375258 ; GCK
0.925 0.080 7 44149986 missense variant C/T snv 4.0E-06 2
rs1018185646
HNF4A
1.000 0.040 20 44428455 missense variant T/C snv 4.0E-06 1
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs750931344
SLC38A4
1.000 0.040 12 46769424 missense variant C/T snv 4.0E-06 1
rs764437500
EHMT1
0.925 0.080 9 137716697 missense variant G/A snv 4.0E-06 2