Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs193922283
GCK
0.851 0.080 7 44145176 missense variant G/A snv 4
rs764232985
GCK
0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 4
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
rs1064794268
GCK
0.925 0.080 7 44153396 missense variant T/G snv 2
rs1286804191
GCK
0.925 0.080 7 44145212 missense variant G/A snv 4.1E-06 2
rs1554335761
GCK
0.925 0.080 7 44152396 missense variant C/T snv 2
rs1562719705
GCK
0.925 0.080 7 44153361 missense variant G/A snv 2
rs193922262
GCK
0.925 0.080 7 44145636 stop gained C/A;G snv 4.3E-06 2
rs193922282
GCK
0.925 0.080 7 44145189 missense variant C/T snv 2
rs193922287
GCK
0.925 0.080 7 44153334 missense variant G/A snv 4.0E-06 2
rs373418736
GCK
0.925 0.080 7 44153306 missense variant C/T snv 2.0E-05 3.5E-05 2
rs556581174
GCK
0.925 0.080 7 44145637 stop gained G/A;C;T snv 2
rs762263694
GCK
0.925 0.080 7 44153403 missense variant G/A snv 1.2E-05 2.8E-05 2
rs777870079
GCK
1.000 0.080 7 44145602 stop gained G/A;T snv 4.3E-06 2
rs104894010
GCK
1.000 0.080 7 44151048 missense variant A/G snv 1
rs104894016
GCK
1.000 0.080 7 44145618 missense variant C/G;T snv 1
rs1057521092
GCK
1.000 0.080 7 44145651 missense variant C/T snv 1
rs1131691416
GCK
1.000 0.080 7 44145194 missense variant C/T snv 1
rs1167124132
GCK
1.000 0.080 7 44145576 missense variant G/A snv 1
rs1176659689
GCK
1.000 0.080 7 44152278 missense variant G/T snv 4.0E-06 1
rs1338970607
GCK
1.000 0.080 7 44152305 missense variant A/G snv 4.0E-06 1
rs1376620210
GCK
1.000 0.080 7 44145600 missense variant C/T snv 1
rs1554334579
GCK
1.000 0.080 7 44145577 missense variant G/T snv 1