Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs1272388614
ABCC8
0.851 0.080 11 17395658 missense variant C/T snv 2.4E-05 3.5E-05 5
rs137852787
PDX1
0.882 0.080 13 27924519 missense variant G/A snv 1.3E-03 2.0E-04 5
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 5
rs1884614
LOC105372629
0.882 0.080 20 44351879 non coding transcript exon variant C/T snv 0.18 5
rs2233580
PAX4
0.882 0.080 7 127613496 missense variant C/T snv 8.2E-03 2.1E-03 5
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 5
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 5
rs753285226
HNF4A
0.882 0.080 20 44406084 missense variant C/A;T snv 4.0E-06 5
rs757110
ABCC8
0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 5
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 5
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs1057520504
HNF1A
0.882 0.080 12 120994238 missense variant G/A snv 4
rs1063538
ADIPOQ ; ADIPOQ-AS1
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs1884051
ESR1
0.882 0.080 6 151962144 intron variant G/A snv 0.60 4
rs2270565
UCP1
0.882 0.080 4 140562317 missense variant T/A snv 8.9E-02 6.5E-02 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs483353044
HNF1A
0.882 0.080 12 120999288 missense variant G/A;C snv 4.9E-04 4
rs7896005
SIRT1
0.925 0.080 10 67891367 intron variant A/G;T snv 0.52; 8.0E-06 0.47 4
rs8192675
SLC2A2
0.925 0.080 3 171007094 intron variant T/C snv 0.42 4
rs9402571 0.882 0.080 6 134167822 downstream gene variant T/G snv 0.22 4
rs952497863
HNF4A
0.925 0.080 20 44414511 missense variant C/T snv 4
rs1051295
KCNB1 ; LOC105372649
0.925 0.080 20 49372368 3 prime UTR variant A/G snv 0.22 3
rs1052717
SREBF2
0.925 0.080 22 41885425 intron variant A/G snv 0.62 3