Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 14
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 7
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7