Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 14
rs3811463
LIN28A
0.752 0.400 1 26427451 3 prime UTR variant T/A;C snv 14
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs5435
SLC2A4
0.851 0.200 17 7283804 missense variant T/A;C snv 0.65 6
rs1223493898
HNF4A
0.851 0.120 20 44406090 missense variant G/A;C snv 5
rs587780345
LOC105375258 ; GCK
0.851 0.080 7 44150004 missense variant C/T snv 5
rs753285226
HNF4A
0.882 0.080 20 44406084 missense variant C/A;T snv 4.0E-06 5
rs833069
VEGFA
0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs952497863
HNF4A
0.925 0.080 20 44414511 missense variant C/T snv 4
rs192902098
PDX1
1.000 0.040 13 27920235 missense variant C/A;G;T snv 2.6E-03; 3.4E-04; 5.6E-05 3
rs5030952
CAPN10
0.925 0.160 2 240603286 intron variant C/G;T snv 3
rs587780346
LOC105375258 ; GCK
0.925 0.080 7 44149823 missense variant T/G snv 3
rs7612463
UBE2E2
0.925 0.080 3 23294959 intron variant C/A;G snv 3
rs736118
STRA6
1.000 0.080 15 74181398 missense variant C/G;T snv 0.16 2
rs10068521
PRLR
5 35230278 5 prime UTR variant G/A;C snv 1