Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057524905
LOC105375258 ; GCK
0.882 0.080 7 44147834 splice acceptor variant C/T snv 3
rs1064793998
GCK
0.882 0.080 7 44153325 missense variant C/T snv 3
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs193922289
GCK
0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 3
rs8004664
FOXN3
0.925 0.080 14 89568628 intron variant G/A;C snv 3
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
rs1385251852
MIR3646 ; HNF4A
0.925 0.080 20 44406208 frameshift variant G/- delins 2
rs1392795567
HNF4A
0.925 0.080 20 44414663 splice donor variant G/A snv 2
rs1562715574
LOC105375258 ; GCK
0.925 0.080 7 44147795 missense variant T/C snv 2
rs1564911425
INS-IGF2 ; INS
0.925 0.080 11 2159895 missense variant G/C snv 2
rs1565886545
HNF1A
0.925 0.080 12 120996261 splice acceptor variant G/A;C snv 2
rs1568724014
MIR3646 ; HNF4A
0.925 0.080 20 44407421 stop gained C/T snv 2
rs193922262
GCK
0.925 0.080 7 44145636 stop gained C/A;G snv 4.3E-06 2
rs193922287
GCK
0.925 0.080 7 44153334 missense variant G/A snv 4.0E-06 2
rs373269573
EHMT1
0.925 0.080 9 137711015 missense variant G/A snv 1.6E-04 9.1E-05 2
rs3738435
CHRM3
0.925 0.080 1 239907303 intron variant T/C snv 0.23 2
rs397514580
GCK ; LOC105375258
0.925 0.080 7 44146467 missense variant C/T snv 2