Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6938256
CDKAL1
6 20887723 intron variant G/A;T snv 1
rs3088440
CDKN2A ; CDKN2A-DT
0.776 0.240 9 21968160 3 prime UTR variant G/A snv 0.13 12
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 5
rs7598922
DHX57
2 38855202 missense variant T/C snv 0.62 0.54 1
rs2021966
ENPP1
1.000 0.080 6 131829299 intron variant A/G snv 0.42 2
rs17466684
EPHX2
0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs1232880706
FBN1
0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs3758539
FFAR4 ; RBP4
0.925 0.120 10 93601831 intron variant C/T snv 0.13 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs16847024
GC
0.882 0.120 4 71784962 intron variant C/T snv 3.2E-02 4
rs3733359
GC
0.925 0.120 4 71784057 splice region variant G/A snv 0.12; 4.2E-06 0.13 3
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs587780343
GCK
7 44145638 missense variant C/A;T snv 1