Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
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
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13