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
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs2236242
SERPINA12
0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs2294021
CCDC22
0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs452204
IL1RN
0.807 0.200 2 113131484 intron variant G/A snv 0.45 7
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs379489
CFH
0.851 0.200 1 196724321 intron variant A/G snv 0.65 4
rs4730751
CAV1
0.882 0.120 7 116540796 intron variant C/A snv 0.22 4
rs730497
GCK ; LOC105375257
0.882 0.160 7 44184122 intron variant G/A snv 0.17 4
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs7588550
ERBB4
0.851 0.160 2 212304043 intron variant G/A snv 0.96 4
rs1033182
ESR1
0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs12434215
RTN1
0.882 0.160 14 59642862 intron variant A/G snv 0.33 3
rs161740
CHD1
0.882 0.200 5 98869326 intron variant C/A;T snv 3