Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1446306735
ABCC8
0.882 0.120 11 17395664 missense variant C/A;T snv 3
rs59852838
ABCC8
0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 3
rs587777042
CYC1
0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 3
rs8004664
FOXN3
0.925 0.080 14 89568628 intron variant G/A;C snv 3
rs1057524902
GCK
0.882 0.080 7 44145495 splice donor variant A/T snv 3
rs1064793998
GCK
0.882 0.080 7 44153325 missense variant C/T snv 3
rs193922289
GCK
0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 3
rs193929375
GCK
0.882 0.120 7 44145560 missense variant C/A snv 3
rs1057524904
LOC105375258 ; GCK
0.882 0.080 7 44147765 missense variant G/A snv 3
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
rs534828104
AHSG
0.925 0.080 3 186618566 missense variant A/G snv 2
rs3738435
CHRM3
0.925 0.080 1 239907303 intron variant T/C snv 0.23 2
rs373269573
EHMT1
0.925 0.080 9 137711015 missense variant G/A snv 1.6E-04 9.1E-05 2
rs764437500
EHMT1
0.925 0.080 9 137716697 missense variant G/A snv 4.0E-06 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
rs1057524906
GCK
0.925 0.080 7 44153387 missense variant A/G snv 2
rs1064794268
GCK
0.925 0.080 7 44153396 missense variant T/G snv 2