Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10139403 1.000 0.040 14 100728224 intron variant A/G snv 0.62 1
rs1018185646 1.000 0.040 20 44428455 missense variant T/C snv 4.0E-06 1
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894006 0.925 0.040 7 44149992 stop gained G/A;T snv 1.2E-05 2
rs1050828 0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
rs10515074 0.925 0.120 5 68270365 intron variant A/G;T snv 2
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
rs1057524902
GCK
0.882 0.080 7 44145495 splice donor variant A/T snv 3
rs1057524903 0.925 0.080 7 44146466 missense variant T/C snv 2
rs1057524904 0.882 0.080 7 44147765 missense variant G/A snv 3
rs1057524905 0.882 0.080 7 44147834 splice acceptor variant C/T snv 3
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
rs1057524908 0.925 0.080 12 120993686 frameshift variant -/C delins 2
rs1064793998
GCK
0.882 0.080 7 44153325 missense variant C/T snv 3
rs1064794268
GCK
0.925 0.080 7 44153396 missense variant T/G snv 2
rs10770125 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs1085307455 0.925 0.080 7 44149977 missense variant G/A;T snv 8.0E-06 2
rs11202592 0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 5
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs11932595 0.827 0.160 4 55457430 intron variant A/G;T snv 12