Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs1799941
SHBG
0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 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
rs2241767
ADIPOQ-AS1 ; ADIPOQ
0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs3774261
ADIPOQ ; ADIPOQ-AS1
0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs727479
MIR4713HG ; CYP19A1 ; MIR4713
0.790 0.240 15 51242350 intron variant C/A;T snv 10
rs2119882
MTNR1A
0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9
rs2236242
SERPINA12
0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 8