Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 8
rs11212617
C11orf65
0.827 0.200 11 108412434 intron variant C/A snv 0.49 7
rs2059807
INSR
0.851 0.200 19 7166098 intron variant A/G;T snv 7
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 7
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 7
rs10818854
DENND1A
0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 6
rs12086634
HSD11B1-AS1 ; HSD11B1
0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs13429458
THADA
0.827 0.200 2 43411699 intron variant A/C snv 0.14 6
rs1887922
IDE
0.851 0.240 10 92464408 intron variant C/T snv 0.85 6
rs2470152
CYP19A1
0.827 0.240 15 51302775 intron variant G/A snv 0.50 6
rs4385527
AOPEP
0.827 0.280 9 94886305 intron variant G/A snv 0.31 6
rs4820599
LRRC75B ; GGT1
0.925 0.160 22 24594246 intron variant A/G snv 0.43 6
rs757343
VDR
0.807 0.360 12 47845892 intron variant C/T snv 0.12 6
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 5
rs12478601
THADA
0.851 0.200 2 43494369 intron variant C/T snv 0.61 5
rs12495941
ADIPOQ
0.851 0.280 3 186850391 intron variant G/T snv 0.35 5
rs9926289
FTO
0.882 0.160 16 53786591 intron variant G/A snv 0.41 5
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 4
rs1569198
DKK1
0.851 0.200 10 52316511 intron variant A/G snv 0.41 0.42 4
rs2479106
DENND1A
0.851 0.120 9 123762933 intron variant A/G snv 0.44 4
rs4844880
HSD11B1-AS1 ; HSD11B1
0.882 0.240 1 209697571 intron variant A/T snv 0.70 4
rs10500204
INSR
0.882 0.160 19 7182952 intron variant A/C snv 0.25 3
rs2252673
INSR
0.882 0.120 19 7150407 intron variant C/G snv 0.75 3