Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9
rs2236242
SERPINA12
0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9