Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63 7
rs9319428
FLT1
0.925 0.080 13 28399484 intron variant G/A snv 0.30 4
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv 4
rs879254535
LDLR
0.925 0.080 19 11105369 missense variant T/A;C;G snv 5
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs8179183
LEPR
1.000 0.080 1 65610269 missense variant G/C;T snv 3
rs805297
BAG6 ; APOM
0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs78338345
GGA3
1.000 0.080 17 75242428 missense variant C/G snv 7.7E-03 2.5E-03 2
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 10
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs771038258
SELENBP1
1 151365837 missense variant A/G snv 8.0E-06 2.1E-05 2
rs770730728
GCK ; LOC105375258
7 44147757 synonymous variant G/A snv 4.0E-06 7.0E-06 1
rs769455
APOE
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9
rs762304200
SHBG
17 7630716 synonymous variant A/G snv 2.8E-05 2
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs7566605
LOC107985940
0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
rs751671151
PLAT
8 42180286 missense variant A/G snv 4.0E-06 1.4E-05 1