Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10139403
DLK1
1.000 0.040 14 100728224 intron variant A/G snv 0.62 1
rs1018185646
HNF4A
1.000 0.040 20 44428455 missense variant T/C snv 4.0E-06 1
rs1410713 1.000 0.040 20 3079704 downstream gene variant A/C snv 0.62 1
rs1447680989
GCKR
1.000 0.040 2 27501147 missense variant G/A snv 4.0E-06 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
rs746913146
LOC105375258 ; GCK
1.000 0.040 7 44149816 missense variant G/A snv 4.0E-06 1
rs750931344
SLC38A4
1.000 0.040 12 46769424 missense variant C/T snv 4.0E-06 1
rs755498926
GCK
1.000 0.040 7 44145228 missense variant T/C snv 4.1E-06 1
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
rs572115942
PHKG2
0.925 0.240 16 30756714 missense variant G/A snv 8.0E-05 7.7E-05 7
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs8004664
FOXN3
0.925 0.080 14 89568628 intron variant G/A;C snv 3
rs104894006
GCK ; LOC105375258
0.925 0.040 7 44149992 stop gained G/A;T snv 1.2E-05 2
rs10515074
PIK3R1
0.925 0.120 5 68270365 intron variant A/G;T snv 2
rs1057524900
GCK
0.925 0.080 7 44145173 missense variant G/A;T snv 4.2E-06 2
rs1057524901
GCK
0.925 0.080 7 44145190 frameshift variant G/- del 2
rs1057524903
GCK ; LOC105375258
0.925 0.080 7 44146466 missense variant T/C snv 2
rs1057524906
GCK
0.925 0.080 7 44153387 missense variant A/G snv 2
rs1057524907
INS-IGF2 ; INS
0.925 0.080 11 2159907 missense variant T/C snv 2
rs1057524908
HNF1A
0.925 0.080 12 120993686 frameshift variant -/C delins 2
rs1064794268
GCK
0.925 0.080 7 44153396 missense variant T/G snv 2
rs1085307455
GCK ; LOC105375258
0.925 0.080 7 44149977 missense variant G/A;T snv 8.0E-06 2
rs1375557127
HNF4A
0.925 0.080 20 44424123 missense variant G/A snv 4.0E-06 2