Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs1410713 1.000 0.040 20 3079704 downstream gene variant A/C snv 0.62 1
rs2770381 1.000 0.040 20 3081340 downstream gene variant A/C snv 0.35 1
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs6084264
AVP
1.000 0.040 20 3089925 upstream gene variant T/C snv 0.58 1
rs1057524905 0.882 0.080 7 44147834 splice acceptor variant C/T snv 3
rs1565886545 0.925 0.080 12 120996261 splice acceptor variant G/A;C snv 2
rs953686324 0.851 0.160 1 16044506 frameshift variant -/G delins 4.3E-06 5.6E-05 7
rs1057524901
GCK
0.925 0.080 7 44145190 frameshift variant G/- del 2
rs1057524908 0.925 0.080 12 120993686 frameshift variant -/C delins 2
rs1385251852 0.925 0.080 20 44406208 frameshift variant G/- delins 2
rs776793516 0.925 0.080 12 120997492 frameshift variant CA/- delins 4.0E-06 2
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs7744 0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs164147 0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs1057524902
GCK
0.882 0.080 7 44145495 splice donor variant A/T snv 3
rs1392795567 0.925 0.080 20 44414663 splice donor variant G/A snv 2
rs518147 0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs11202592 0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 5
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs2273773 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs340874 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7