Disease: Hyperglycemia
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 14
rs267607555
LMNA
0.807 0.280 1 156136009 missense variant C/T 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
rs137853238
HNF1A
0.807 0.200 12 120994265 missense variant G/A snv 3
rs369841551
MC4R
0.882 0.120 18 60371884 stop gained G/A;T snv 4.0E-06 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
rs764232985
GCK
0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 2