Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1049673
CD36
0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs3813929
HTR2C
0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5
rs33954001
LOC105373000 ; SLC5A1
1.000 0.120 22 32110063 missense variant C/G;T snv 4.8E-02; 2.4E-05 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs997509
ENPP1
0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
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
rs587783672
KCNJ11
0.882 0.080 11 17387413 missense variant C/T snv 4.0E-06 5
rs867232360
GCK
1.000 0.040 7 44145552 missense variant C/T snv 3
rs11061946
ADIPOR2
1.000 0.080 12 1719361 intron variant C/T snv 6.8E-02 2
rs3731201
CDKN2A
1.000 0.080 9 21988897 intron variant C/T snv 0.86 2
rs935907949
SH2B1
16 28867355 missense variant C/T snv 7.0E-06 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs75527207
CFTR
0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15
rs1801483
GCGR
0.851 0.160 17 81809839 missense variant G/A snv 7.4E-03 6.3E-03 7
rs137852787
PDX1
0.882 0.080 13 27924519 missense variant G/A snv 1.3E-03 2.0E-04 5