Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587780345
LOC105375258 ; GCK
0.851 0.080 7 44150004 missense variant C/T snv 5
rs193922283
GCK
0.851 0.080 7 44145176 missense variant G/A snv 4
rs193922331
LOC105375258 ; GCK
0.882 0.080 7 44147726 missense variant A/G snv 7.0E-06 4
rs1057524902
GCK
0.882 0.080 7 44145495 splice donor variant A/T snv 3
rs1057524904
LOC105375258 ; GCK
0.882 0.080 7 44147765 missense variant G/A snv 3
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 2
rs1064794268
GCK
0.925 0.080 7 44153396 missense variant T/G snv 2
rs1562715574
LOC105375258 ; GCK
0.925 0.080 7 44147795 missense variant T/C snv 2
rs1562719705
GCK
0.925 0.080 7 44153361 missense variant G/A snv 2
rs556581174
GCK
0.925 0.080 7 44145637 stop gained G/A;C;T snv 2
rs104894009
LOC105375258 ; GCK
0.882 0.120 7 44146587 missense variant C/G snv 1
rs104894010
GCK
1.000 0.080 7 44151048 missense variant A/G snv 1
rs104894011
GCK ; LOC105375258
1.000 0.080 7 44147720 stop gained C/A;T snv 1
rs104894016
GCK
1.000 0.080 7 44145618 missense variant C/G;T snv 1
rs1312678560
GCK ; LOC105375258
1.000 0.080 7 44146574 missense variant C/A;T snv 7.0E-06 1
rs1554334579
GCK
1.000 0.080 7 44145577 missense variant G/T snv 1
rs1554334886
LOC105375258 ; GCK
1.000 0.080 7 44146541 missense variant A/G snv 1
rs1554335391
LOC105375258 ; GCK
1.000 0.080 7 44149758 splice region variant CCAC/- delins 1
rs1554335612
GCK
1.000 0.080 7 44151068 missense variant T/A snv 1
rs1554335616
GCK
1.000 0.080 7 44151075 missense variant G/C;T snv 1
rs1554335752
GCK
1.000 0.080 7 44152339 frameshift variant A/- del 1
rs1554335954
GCK
1.000 0.080 7 44153411 missense variant A/G;T snv 1
rs193921340
GCK
1.000 0.080 7 44145581 missense variant A/G;T snv 1
rs193921400
LOC105375258 ; GCK
1.000 0.080 7 44147755 missense variant A/C;G snv 1