Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057524905 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 3
rs193922289
GCK
0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 3
rs587777042 0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 3
rs1568724014 0.925 0.080 20 44407421 stop gained C/T snv 2
rs397514580 0.925 0.080 7 44146467 missense variant C/T snv 2
rs751279776 0.925 0.080 7 44149986 missense variant C/T snv 4.0E-06 2
rs2282018
AVP
1.000 0.040 20 3084303 intron variant C/T snv 0.60 1
rs750931344 1.000 0.040 12 46769424 missense variant C/T snv 4.0E-06 1
rs776793516 0.925 0.080 12 120997492 frameshift variant CA/- delins 4.0E-06 2
rs1057524901
GCK
0.925 0.080 7 44145190 frameshift variant G/- del 2
rs1385251852 0.925 0.080 20 44406208 frameshift variant G/- delins 2
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs137853240 0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs572115942 0.925 0.240 16 30756714 missense variant G/A snv 8.0E-05 7.7E-05 7
rs137853238 0.807 0.200 12 120994265 missense variant G/A snv 6
rs1057524904 0.882 0.080 7 44147765 missense variant G/A snv 3
rs1375557127 0.925 0.080 20 44424123 missense variant G/A snv 4.0E-06 2
rs1392795567 0.925 0.080 20 44414663 splice donor variant G/A snv 2
rs1564865302 0.925 0.040 11 17387395 missense variant G/A 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
rs764437500 0.925 0.080 9 137716697 missense variant G/A snv 4.0E-06 2
rs1447680989 1.000 0.040 2 27501147 missense variant G/A snv 4.0E-06 1