Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777893
MTOR
0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs866294686
TRIM8 ; LOC105378460
0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs1400419650
TRIP11
0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 38
rs1555386022
TRIP11
0.708 0.320 14 92003418 splice donor variant C/A snv 38
rs1232880706
FBN1
0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1034395178
LZTR1
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06 33
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 13
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 11
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 11
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 11
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 10
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 10
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 10
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 8
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 7