Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 8
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs3745367
RETN
0.827 0.200 19 7669625 intron variant G/A snv 0.39 8
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 7
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs1884613
LOC105372629
0.807 0.200 20 44351775 intron variant C/A;G;T snv 7
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 7
rs5030728
TLR4
0.807 0.160 9 117712004 intron variant G/A;T snv 0.23 7
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 7
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs11722228
SLC2A9
0.851 0.160 4 9914117 intron variant C/T snv 0.32 6
rs12086634
HSD11B1-AS1 ; HSD11B1
0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 6
rs7204609
FTO
0.827 0.200 16 53799693 intron variant T/C snv 0.14 6
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs8064821
SOCS3 ; LOC101928674
0.851 0.120 17 78361310 intron variant C/A snv 0.17 6
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6