Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064794268
GCK
0.925 0.080 7 44153396 missense variant T/G snv 2
rs1057524906
GCK
0.925 0.080 7 44153387 missense variant A/G snv 2
rs764232985
GCK
0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 4
rs193922287
GCK
0.925 0.080 7 44153334 missense variant G/A snv 4.0E-06 2
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
rs104894006
GCK ; LOC105375258
0.925 0.040 7 44149992 stop gained G/A;T snv 1.2E-05 2
rs751279776
LOC105375258 ; GCK
0.925 0.080 7 44149986 missense variant C/T snv 4.0E-06 2
rs1085307455
GCK ; LOC105375258
0.925 0.080 7 44149977 missense variant G/A;T snv 8.0E-06 2
rs746913146
LOC105375258 ; GCK
1.000 0.040 7 44149816 missense variant G/A snv 4.0E-06 1
rs1057524905
LOC105375258 ; GCK
0.882 0.080 7 44147834 splice acceptor variant C/T snv 3
rs1562715574
LOC105375258 ; GCK
0.925 0.080 7 44147795 missense variant T/C snv 2
rs1057524904
LOC105375258 ; GCK
0.882 0.080 7 44147765 missense variant G/A snv 3
rs193922331
LOC105375258 ; GCK
0.882 0.080 7 44147726 missense variant A/G snv 7.0E-06 4
rs397514580
GCK ; LOC105375258
0.925 0.080 7 44146467 missense variant C/T snv 2
rs1057524903
GCK ; LOC105375258
0.925 0.080 7 44146466 missense variant T/C snv 2
rs556581174
GCK
0.925 0.080 7 44145637 stop gained G/A;C;T snv 2
rs193922262
GCK
0.925 0.080 7 44145636 stop gained C/A;G snv 4.3E-06 2
rs193929375
GCK
0.882 0.120 7 44145560 missense variant C/A snv 3
rs1057524902
GCK
0.882 0.080 7 44145495 splice donor variant A/T snv 3
rs755498926
GCK
1.000 0.040 7 44145228 missense variant T/C snv 4.1E-06 1
rs1057524901
GCK
0.925 0.080 7 44145190 frameshift variant G/- del 2
rs1057524900
GCK
0.925 0.080 7 44145173 missense variant G/A;T snv 4.2E-06 2
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11