Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10770125 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs193922331 0.882 0.080 7 44147726 missense variant A/G snv 7.0E-06 4
rs561017686 0.882 0.120 2 181678138 missense variant G/A;C snv 8.0E-06; 8.4E-04 4
rs764232985
GCK
0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 4
rs1057524904 0.882 0.080 7 44147765 missense variant G/A snv 3
rs1064793998
GCK
0.882 0.080 7 44153325 missense variant C/T snv 3
rs1446306735 0.882 0.120 11 17395664 missense variant C/A;T snv 3
rs193922289
GCK
0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 3
rs193929375
GCK
0.882 0.120 7 44145560 missense variant C/A snv 3
rs587777042 0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 3
rs59852838 0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 3
rs1057524900
GCK
0.925 0.080 7 44145173 missense variant G/A;T snv 4.2E-06 2
rs1057524903 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 0.925 0.080 11 2159907 missense variant T/C snv 2
rs1064794268
GCK
0.925 0.080 7 44153396 missense variant T/G snv 2
rs1085307455 0.925 0.080 7 44149977 missense variant G/A;T snv 8.0E-06 2
rs1375557127 0.925 0.080 20 44424123 missense variant G/A snv 4.0E-06 2
rs1562715574 0.925 0.080 7 44147795 missense variant T/C snv 2
rs1564865302 0.925 0.040 11 17387395 missense variant G/A snv 2
rs1564911425 0.925 0.080 11 2159895 missense variant G/C snv 2
rs193922287
GCK
0.925 0.080 7 44153334 missense variant G/A snv 4.0E-06 2
rs373269573 0.925 0.080 9 137711015 missense variant G/A snv 1.6E-04 9.1E-05 2
rs397514580 0.925 0.080 7 44146467 missense variant C/T snv 2
rs534828104 0.925 0.080 3 186618566 missense variant A/G snv 2