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
rs1057524908
HNF1A
0.925 0.080 12 120993686 frameshift variant -/C delins 2
rs1565886545
HNF1A
0.925 0.080 12 120996261 splice acceptor variant G/A;C snv 2
rs776793516
HNF1A
0.925 0.080 12 120997492 frameshift variant CA/- delins 4.0E-06 2
rs1375557127
HNF4A
0.925 0.080 20 44424123 missense variant G/A snv 4.0E-06 2
rs1392795567
HNF4A
0.925 0.080 20 44414663 splice donor variant G/A snv 2
rs1057524907
INS-IGF2 ; INS
0.925 0.080 11 2159907 missense variant T/C snv 2
rs1564911425
INS-IGF2 ; INS
0.925 0.080 11 2159895 missense variant G/C snv 2
rs1564865302
KCNJ11
0.925 0.040 11 17387395 missense variant G/A snv 2
rs1562715574
LOC105375258 ; GCK
0.925 0.080 7 44147795 missense variant T/C snv 2
rs751279776
LOC105375258 ; GCK
0.925 0.080 7 44149986 missense variant C/T snv 4.0E-06 2
rs1385251852
MIR3646 ; HNF4A
0.925 0.080 20 44406208 frameshift variant G/- delins 2
rs1568724014
MIR3646 ; HNF4A
0.925 0.080 20 44407421 stop gained C/T snv 2
rs10515074
PIK3R1
0.925 0.120 5 68270365 intron variant A/G;T snv 2
rs9906827
RPTOR
0.925 0.120 17 80691605 intron variant C/A;T snv 2
rs8066560
SREBF1
0.925 0.040 17 17824729 intron variant A/G snv 0.64 2
rs1446306735
ABCC8
0.882 0.120 11 17395664 missense variant C/A;T snv 3
rs59852838
ABCC8
0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 3
rs587777042
CYC1
0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 3
rs8004664
FOXN3
0.925 0.080 14 89568628 intron variant G/A;C snv 3
rs1057524902
GCK
0.882 0.080 7 44145495 splice donor variant A/T snv 3
rs1064793998
GCK
0.882 0.080 7 44153325 missense variant C/T snv 3
rs193922289
GCK
0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 3
rs193929375
GCK
0.882 0.120 7 44145560 missense variant C/A snv 3
rs1057524904
LOC105375258 ; GCK
0.882 0.080 7 44147765 missense variant G/A snv 3