Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057524905
LOC105375258 ; GCK
0.882 0.080 7 44147834 splice acceptor variant C/T snv 3
rs369841551
MC4R
0.882 0.120 18 60371884 stop gained G/A;T snv 4.0E-06 3
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs764232985
GCK
0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 4
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs10770125
INS-IGF2 ; IGF2 ; IGF2-AS
0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs193922331
LOC105375258 ; GCK
0.882 0.080 7 44147726 missense variant A/G snv 7.0E-06 4
rs13412852
LPIN1
0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs561017686
NEUROD1 ; CERKL
0.882 0.120 2 181678138 missense variant G/A;C snv 8.0E-06; 8.4E-04 4
rs1272388614
ABCC8
0.851 0.080 11 17395658 missense variant C/T snv 2.4E-05 3.5E-05 5
rs146488435
KCNH6
0.851 0.080 17 63533914 missense variant C/G;T snv 8.0E-06; 6.4E-05 5
rs11202592
KLLN ; PTEN
0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 5
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs137853238
HNF1A
0.807 0.200 12 120994265 missense variant G/A snv 6
rs267607555
LMNA
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs953686324
CLCNKB
0.851 0.160 1 16044506 frameshift variant -/G delins 4.3E-06 5.6E-05 7
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs572115942
PHKG2
0.925 0.240 16 30756714 missense variant G/A snv 8.0E-05 7.7E-05 7
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs80356618
KCNJ11
0.807 0.200 11 17387595 missense variant C/A;T snv 8
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10